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Mutation screening and genotype phenotype correlation of α-crystallin, γ-crystallin and GJA8 gene in congenital cataract

PURPOSE: To screen α-crystallin (CRYAB), γ-crystallin (CRYGC and CRYGD), and Connexin 50 (Cx-50 or GJA8) genes in congenital cataract patients and controls. METHODS: Thirty clinically diagnosed congenital cataract cases below 3 years of age from northern India, presenting at Dr. R. P. Centre for Oph...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Kumar, Manoj, Agarwal, Tushar, Khokhar, Sudarshan, Kaur, Punit, Roy, Tara Sankar, Dada, Rima
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Molecular Vision 2011
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3060158/
https://ncbi.nlm.nih.gov/pubmed/21423869
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