Macular pattern retinal dystrophy, adult-onset diabetes, and deafness: a family study of A3243G mitochondrial heteroplasmy (Q44028130)

29 November 2017

title

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

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29 November 2017

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T J Harrison

1

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29 November 2017

R G Boles

2

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29 November 2017

D R Johnson

3

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29 November 2017

C LeBlond

4

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29 November 2017

L J Wong

5

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29 November 2017

language of work or name

English

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publication date

1 August 1997

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American Journal of Ophthalmology

29 November 2017

published in

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29 November 2017

volume

124

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29 November 2017

issue

2

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29 November 2017

page(s)

217-221

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The retinal manifestations of mitochondrial myopathy. A study of 22 cases

29 November 2017

cites work

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7 January 2021

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Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene

7 January 2021

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Macular pattern dystrophy associated with a mutation of mitochondrial DNA.

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A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies

7 January 2021

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Rapid and noninvasive screening of patients with mitochondrial myopathy

7 January 2021

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Leber's hereditary optic neuropathy and Kearns-Sayre syndrome: mitochondrial DNA mutations

7 January 2021

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Adult-onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNA(Leu(UUR)) mutation

7 January 2021

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Pattern Dystrophy of the Retinal Pigment Epithelium

7 January 2021

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Pigment epithelial pattern dystrophy. Four different manifestations in a family

7 January 2021

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7 January 2021

Identifiers

DOI

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29 November 2017

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