The epidemiology and genetics of vitiligo (Q41665553)

6 October 2017

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title

The epidemiology and genetics of vitiligo (English)

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6 October 2017

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Nordlund JJ

1

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6 October 2017

publication date

1 November 1997

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6 October 2017

published in

Clinics in Dermatology

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6 October 2017

volume

15

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6 October 2017

issue

6

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6 October 2017

page(s)

875-878

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Studies on vitiligo. I. Epidemiological profile in Calcutta, India

6 October 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

Occupational vitiligo: clinical and epidemiological aspects

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

Secretion of blood group specific substances in saliva of vitiligo patients. A preliminary report

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https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

ABO blood groups and vitiligo

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

Secretory State in Vitiligo

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

Genetic association in vitiligo: ABO, MNSs, Rhesus, Kell and Duffy blood groups.

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

Vitiligo is associated with a significant increase in HLA-A30, Cw6 and DQw3 and a decrease in C4AQ0 in northern Italian patients

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

Study of HLA class I/IL and T lymphocyte subsets in Kuwaiti vitiligo patients

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

Age of onset in vitiligo: relationship with HLA supratypes.

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

Difference in clinical features and HLA antigens between familial and non-familial vitiligo of non-segmental type

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

Studies on vitiligo. II. Familial aggregation and genetics

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

A mouse model for vitiligo.

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

The vit gene maps to the mi (microphthalmia) locus of the laboratory mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

A gene for Waardenburg syndrome type 2 maps close to the human homologue of the microphthalmia gene at chromosome 3p12-p14.1.

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotypic consequences.

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

Cloning of MITF, the human homolog of the mouse microphthalmia gene and assignment to chromosome 3p14.1-p12.3.

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

The mutational spectrum in Waardenburg syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q.

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

Retinitis pigmentosa, hearing loss and vitiligo: report of two patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

Progressive spastic paraparesis, vitiligo, premature graying, and distinct facial appearance: a new genetic syndrome in 3 sibs

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

Linkage analysis in a large kindred with autosomal dominant transmission of polyglandular autoimmune disease type II (Schmidt syndrome).

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

Vitiligo patterns simulating autoimmune and rheumatic diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

Unstable mutations in vitiligo, organ-specific autoimmune diseases, and multiple endocrine adenoma/peptic-ulcer syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

A family study of vitiligo patterns

1 reference

https://api.crossref.org/works/10.1016%2FS0738-081X%2897%2900128-4

7 January 2021

10.1016/S0738-081X(97)00128-4

Identifiers

DOI

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release_jlei27bm2vbfjghkypmx4fqaoa

6 October 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/jlei27bm2vbfjghkypmx4fqaoa

24 November 2022

mapped directly with Wikidata item

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