Mutation Analysis of 63 Northwest Chinese Probands with Oculocutaneous Albinism

Sporadic Hirschsprung Disease: Mutational Spectrum and Novel Candidate Genes Revealed by Next-generation Sequencing

(2017) Zhen Zhang et al.   Scientific Reports

Molecular outcomes, clinical consequences and genetic diagnosis of Oculocutaneous Albinism in Pakistani population

(2017) Mohsin Shahzad et al.   Scientific Reports

Prenatal Genotyping of Four Common Oculocutaneous Albinism Genes in 51 Chinese Families

(2015) Ai-Hua Wei et al.   Journal of Genetics and Genomics

Molecular analysis of Korean patients with oculocutaneous albinism

(2011) Shin Hae Park et al.   JAPANESE JOURNAL OF OPHTHALMOLOGY

Comprehensive analysis of the molecular basis of oculocutaneous albinism in Indian patients lacking a mutation in the tyrosinase gene

(2010) M. Sengupta et al.   BRITISH JOURNAL OF DERMATOLOGY

Tyrosinase gene (TYR) mutations in Chinese patients with oculocutaneous albinism type 1

(2009) Jing Liu et al.   CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY

A Comprehensive Analysis Reveals Mutational Spectra and Common Alleles in Chinese Patients with Oculocutaneous Albinism

(2009) Aihua Wei et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

Recent advances in genetic analyses of oculocutaneous albinism types 2 and 4

(2008) Tamio Suzuki et al.   JOURNAL OF DERMATOLOGICAL SCIENCE

Comprehensive Analysis of Oculocutaneous Albinism among Non-Hispanic Caucasians Shows that OCA1 Is the Most Prevalent OCA Type

(2008) Saunie M. Hutton et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

Molecular diagnosis of oculocutaneous albinism: new mutations in the OCA1-4 genes and practical aspects

(2008) Caroline Rooryck et al.   Pigment Cell & Melanoma Research