Fine mapping of new glaucoma locus GLC1M and exclusion of neuregulin 2 as the causative gene

PURPOSE: We recently identified a novel glaucoma locus on 5q22.1-q32, designated as GLC1M, in a family from the Philippines with autosomal dominant juvenile-onset primary open angle glaucoma (JOAG). No mutations in myocilin (MYOC), optineurin (OPTN), and WD-repeat protein 36 (WDR36) were found. Neur...

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Detalles Bibliográficos
Autores principales: Fan, Bao Jian, Ko, Wendy Charles, Wang, Dan Yi, Canlas, Oscar, Ritch, Robert, Lam, Dennis S. C., Pang, Chi Pui
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2007
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2768763/
https://www.ncbi.nlm.nih.gov/pubmed/17563728

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