Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community. (Q45800793)

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scientific article published on 6 May 2013

Thyroid dyshormonogenesis is mainly caused byTPOmutations in consanguineous community

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English	Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community.	scientific article published on 6 May 2013	Thyroid dyshormonogenesis is mainly caused byTPOmutations in consanguineous community

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scholarly article

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20 February 2020

Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community (English)

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20 February 2020

Thyroid dyshormonogenesis

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based on heuristic

inferred from title

Alvaro Olivera-Nappa

3

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20 February 2020

Nadia Schoenmakers

5

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20 February 2020

Timothy Barrett

18

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20 February 2020

author name string

Hakan Cangul

1

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20 February 2020

Zehra Aycan

2

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20 February 2020

Halil Saglam

4

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20 February 2020

Kristien Boelaert

6

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20 February 2020

Semra Cetinkaya

7

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20 February 2020

Omer Tarim

8

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20 February 2020

Ece Bober

9

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20 February 2020

Feyza Darendeliler

10

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20 February 2020

Veysel Bas

11

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20 February 2020

Korcan Demir

12

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20 February 2020

Banu K Aydin

13

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20 February 2020

Michaela Kendall

14

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20 February 2020

Trevor Cole

15

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20 February 2020

Wolfgang Högler

16

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20 February 2020

V Krishna K Chatterjee

17

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20 February 2020

Eamonn R Maher

19

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20 February 2020

publication date

6 May 2013

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20 February 2020

Clinical Endocrinology

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20 February 2020

79

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20 February 2020

275-281

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20 February 2020

2

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20 February 2020

Defects of thyroidal hydrogen peroxide generation in congenital hypothyroidism

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12127

21 January 2018

Genetics and phenomics of hypothyroidism and goiter due to thyroglobulin mutations

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12127

21 January 2018

Genetic causes of congenital hypothyroidism due to dyshormonogenesis

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12127

21 January 2018

Genetics of congenital hypothyroidism

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12127

21 January 2018

Genetics and phenomics of hypothyroidism and goiter due to TPO mutations

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12127

21 January 2018

Molecular Analysis of the Pds Gene in Pendred Syndrome (Sensorineural Hearing Loss and Goitre)

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12127

21 January 2018

Thyroperoxidase gene mutations in congenital goitrous hypothyroidism with total and partial iodide organification defect

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12127

21 January 2018

Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goiter

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12127

21 January 2018

Identification of five novel inactivating mutations in the human thyroid peroxidase gene by denaturing gradient gel electrophoresis

1 reference

https://api.crossref.org/works/10.1111%2FCEN.12127

21 January 2018

Identifiers

10.1111/CEN.12127

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23236987%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

1 reference

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20 February 2020

ResearchGate publication ID

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