Title : A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent.

Pub. Date : 2016

PMID : 27508083






2 Functional Relationships(s)
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1 In conclusion, we identified a total of 11 mutations, reconfirming the genetic heterogeneity of CYP1B1 in the pathogenesis of PCG. pcg cytochrome P450 family 1 subfamily B member 1 Homo sapiens
2 To the best of our knowledge, this is the largest study investigating the contribution of CYP1B1 to the pathogenesis of PCG in the Pakistani population. pcg cytochrome P450 family 1 subfamily B member 1 Homo sapiens