Title : CYP1B1 gene mutations causing primary congenital glaucoma in Tunisia.

Pub. Date : 2014 Jul

PMID : 24942078






2 Functional Relationships(s)
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Protein Name
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1 This study sought to determine the frequency of CYP1B1 (cytochrome P450, family 1, subfamily B, polypeptide 1) mutations in 18 PCG patients, recruited from Central and Southern of Tunisia. pcg cytochrome P450 family 1 subfamily B member 1 Homo sapiens
2 This study sought to determine the frequency of CYP1B1 (cytochrome P450, family 1, subfamily B, polypeptide 1) mutations in 18 PCG patients, recruited from Central and Southern of Tunisia. pcg cytochrome P450 family 1 subfamily B member 1 Homo sapiens