Analysis of 126 Filipino cases and 218 controls revealed a borderline significant association between RFC1 gene and nsCL/P. 23 Wang et al in a Chinese population, 20 Girardi et al in Italian population 21 and Lakkakula et al in south Indian population 22 indicated that the RFC1 gene variant increases occurrence risk of nsCL/P.
← all excerpts
The study of association between reduced folate carrier 1 (<i>RFC1</i>) polymorphism and non-syndromic cleft lip/palate in Iranian population.
1
—
—