Associated Papers
Novel pathogenic OCRL mutations and genotype-phenotype analysis of Chinese children affected by oculocerebrorenal syndrome: two cases and a literature review.
Zhang Y et al.
Bmc Medical Genomics, 2021
Novel OCRL1 gene mutations in six Chinese families with Lowe syndrome.
Gao Y et al.
World Journal of Pediatrics : Wjp, 2016
Review Recent progress in identification and characterization of loci associated with sex-linked congenital cataract.
Zhang DD et al.
Genetics and Molecular Research : Gmr, 2016
Novel mutation of OCRL1 in Lowe syndrome.
Liu T et al.
Indian Journal of Pediatrics, 2015
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