Retinitis Pigmentosa and Progressive Sensorineural Hearing Loss Caused by a C12258A Mutation in the Mitochondrial MTTS2 Gene-Reference-Cited by-同舟云学术

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Retinitis Pigmentosa and Progressive Sensorineural Hearing Loss Caused by a C12258A Mutation in the Mitochondrial MTTS2 Gene

Published:1999-04 Issue:4 Volume:64 Page:971-985
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Mansergh Fiona C.,Millington-Ward Sophia,Kennan Avril,Kiang Anna-Sophia,Humphries Marian,Farrar G. Jane,Humphries Peter,Kenna Paul F.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference55 articles.

1. Sequence and organization of the human mitochondrial genome;Anderson;Nature,1981

2. A computer program to make analysis with LIPED and LINKAGE easier to perform and less prone to input errors;Attwood;Ann Hum Genet,1988

3. Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion;Ballinger;Nat Genet,1992

4. Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency;Bourgeron;Nat Genet,1995

5. A newly identified locus for Usher syndrome type 1, USH1E, maps to chromosome 21q21;Chaib;Hum Mol Genet,1997

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