Screening of the LTBP2 gene in a north Indian population with primary congenital glaucoma

PURPOSE: Primary congenital glaucoma (PCG), a severe form of glaucoma that presents early in life, is an autosomal recessive eye disorder that results from defects in anterior eye segment. Null mutations in LTBP2 were reported in patients with PCG in Pakistani and Iranian families. This study was ai...

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Detalles Bibliográficos
Autores principales: Mohanty, Kuldeep, Tanwar, Mukesh, Dada, Rima, Dada, Tanuj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3559091/
https://www.ncbi.nlm.nih.gov/pubmed/23378721

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3559091/
https://www.ncbi.nlm.nih.gov/pubmed/23378721

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