Segregation of a PRKCG Mutation in Two RP11 Families-Reference-Cited by-同舟云学术

Segregation of a PRKCG Mutation in Two RP11 Families

Published:1998-05 Issue:5 Volume:62 Page:1248-1252
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Al-Maghtheh Mai,Vithana Eranga N.,Inglehearn Chris F.,Moore Tony,Bird Alan C.,Bhattacharya Shomi S.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference22 articles.

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2. Evidence for a major retinitis pigmentosa locus on 19q13.4 (RP11), and association with a unique bimodal expressivity phenotype;Al-Maghtheh;Am J Hum Genet,1996

3. Retinal photoreceptor dystrophies;Bird;Am J Ophthalmol,1995

4. Impared motor coordination correlates with persistent multiple climbing fiber innervation in PKCγ mutant mice;Chen;Cell,1995

5. A homozygous 1–base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese;Fuchs;Nat Genet,1995

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