Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness (Q60609066)

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13 December 2019

title

Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness. GEDIAM Group (English)

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13 December 2019

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4

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13 December 2019

Sophie Caillat-Zucman

7

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13 December 2019

Alain Gaudric

10

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author name string

P Massin

1

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13 December 2019

M Virally-Monod

2

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13 December 2019

B Vialettes

3

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13 December 2019

H Gin

5

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13 December 2019

B Porokhov

6

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P Froguel

8

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V Paquis-Fluckinger

9

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P J Guillausseau

11

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13 December 2019

publication date

1 September 1999

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13 December 2019

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13 December 2019

volume

106

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13 December 2019

issue

9

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page(s)

1821-1827

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Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

13 December 2019

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Macular pattern dystrophy associated with a mutation of mitochondrial DNA.

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A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

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Maternally inherited diabetes and deafness: a new diabetes subtype

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Prevalence of maternally inherited diabetes and deafness in diabetic populations in the Netherlands

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Extra-pancreatic manifestations in diabetes secondary to mitochondrial DNA point mutation within the tRNALeu(UUR) gene

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Macular pattern retinal dystrophy, adult-onset diabetes, and deafness: a family study of A3243G mitochondrial heteroplasmy

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Macular pattern dystrophy in patients with deafness and diabetes

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Pigmentary retinopathy associated with the mitochondrial DNA 3243 point mutation

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Does mitochondrial genome mutation in subjects with maternally inherited diabetes and deafness decrease severity of diabetic retinopathy?

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Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS)

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Relationship of duration and onset of diabetes to prevalence of diabetic retinopathy.

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Macular dystrophy, diabetes, and deafness associated with a large mitochondrial DNA deletion

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Could coenzyme Q10 and L-carnitine be a treatment for diabetes secondary to 3243 mutation of mtDNA?

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7 January 2021

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7 January 2021

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Identifiers

DOI

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13 December 2019

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