A novel mutation in the CYP4V2 gene in a Chinese patient with Bietti’s crystalline dystrophy

Identification of CYP4V2 mutation in 21 families and overview of mutation spectrum in Bietti crystalline corneoretinal dystrophy

(2011) Xueshan Xiao et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Focus on Molecules: Cytochrome P450 family 4, subfamily V, polypeptide 2 (CYP4V2)

(2011) Donna S. Mackay et al.   EXPERIMENTAL EYE RESEARCH

Finding Homes for Orphan Cytochrome P450s: CYP4V2 and CYP4F22 in Disease States

(2011) E. J. Kelly et al.   MOLECULAR INTERVENTIONS

An Atypical Form of Bietti Crystalline Dystrophy

(2011) Settimio Rossi et al.   OPHTHALMIC GENETICS

Expression and Characterization of CYP4V2 as a Fatty Acid  -Hydroxylase

(2009) M. Nakano et al.   DRUG METABOLISM AND DISPOSITION

Novel CYP4V2 Gene Mutation in a Mexican Patient with Bietti's Crystalline Corneoretinal Dystrophy

(2008) Juan C. Zenteno et al.   CURRENT EYE RESEARCH