Novel mutations in the γ-crystallin genes cause autosomal dominant congenital cataracts

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Bibliographic Details
Published inJournal of medical genetics Vol. 39; no. 5; pp. 352 - 358
Main Authors Santhiya, S T, Shyam Manohar, M, Rawlley, D, Vijayalakshmi, P, Namperumalsamy, P, Gopinath, P M, Löster, J, Graw, J
Format Journal Article
LanguageEnglish
Published London BMJ Publishing Group Ltd 01.05.2002
BMJ
BMJ Group
Subjects
Adolescent
Base Sequence
Biological and medical sciences
cataract
Cataract - genetics
Cataract - pathology
Child
Child, Preschool
Crystallins - genetics
Genetic Predisposition to Disease
Humans
India
Infant
Lens diseases
Letter to JMG
Medical sciences
Mutation
Ophthalmology
Pedigree
polymorphism
Polymorphism, Genetic
Prospective Studies
γ-crystallin
India
Eye disease
Cataract
Lens disease
Congenital
Gene
Autosomal character
Dominant character
Mutation
Anterior segment disease
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Bibliography:href:jmedgenet-39-352.pdf
PMID:12011157
istex:B2FE903A65CFED6048E841CA2C58953811F99C02
ark:/67375/NVC-4QWDR9CH-M
Correspondence to:
 Professor J Graw, GSF-National Research Centre for Environment and Health, Institute of Mammalian Genetics, D-85764 Neuherberg, Germany;
 graw@gsf.de
local:0390352
SourceType-Other Sources-1
content type line 63
ObjectType-Correspondence-1
ObjectType-Commentary-2
ISSN:0022-2593
1468-6244
1468-6244
DOI:10.1136/jmg.39.5.352