The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes

Aims: Multiple genetic causes of congenital cataract have been identified, both as a component of syndromes and in families that present with isolated congenital cataract. Linkage analysis was used to map the genetic locus in a six generation Australian family presenting with total congenital catara...

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Detalhes bibliográficos
Main Authors: McKay, J D, Patterson, B, Craig, J E, Russell-Eggitt, I M, Wirth, M G, Burdon, K P, Hewitt, A W, Cohn, A C, Kerdraon, Y, Mackey, D A
Formato: Artigo
Idioma:Inglês
Publicado em: Copyright 2005 British Journal of Ophthalmology 2005
Assuntos:
Clinical Science - Scientific Reports
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1772710/
https://ncbi.nlm.nih.gov/pubmed/15965161
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bjo.2004.058495
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