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Shin J, Noh JR, Chang DH, Kim YH, Kim MH, Lee ES, et al
In support of this, patients carrying the L232P mutation in CYP51A1 presented with congenital cataracts, neonatal cholestatic jaundice, elevated liver enzymes, and hyperferritinemia, indicating that CYP51A1 mutations may underlie a syndromic disorder affecting both ocular and hepatic systems
Is it okay to consume excessive protein
Presented for research literature review only Eltayeb MM et al
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