Evaluating the association of bone morphogenetic protein 4-V152A and SIX homeobox 6-H141N polymorphisms with congenital cataract and microphthalmia in Western Indian population

BACKGROUND: Congenital cataract and microphthalmia are highly heterogeneous congenital eye disorders that affect normal vision. Although mutation in several genes has been shown to cause congenital cataract and microphthalmia, genetic studies associating single-nucleotide polymorphisms with these co...

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Detalles Bibliográficos
Autores principales: Vidya, NG, Vasavada, AR, Rajkumar, S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5954819/
https://www.ncbi.nlm.nih.gov/pubmed/29692399
http://dx.doi.org/10.4103/jpgm.JPGM_219_17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5954819/
https://www.ncbi.nlm.nih.gov/pubmed/29692399
http://dx.doi.org/10.4103/jpgm.JPGM_219_17

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