Associated Papers
Identification and Computational Analysis of Novel TYR and SLC45A2 Gene Mutations in Pakistani Families With Identical Non-syndromic Oculocutaneous Albinism.
Bibi N et al.
Frontiers in Genetics, 2020
32849781 (PubMed )
Supplement: Data_Sheet_2.docx
Melanotic Malignant Melanoma in Oculocutaneous Albinism Type 4.
Ozaki S et al.
Acta Dermato-venereologica, 2017
Clinical evaluation and molecular screening of a large consecutive series of albino patients.
Mauri L et al.
Journal of Human Genetics, 2017
Deleterious nonsynonymous single nucleotide polymorphisms in human solute carriers: the first comparison of three prediction methods.
Hao DC et al.
European Journal of Drug Metabolism and Pharmacokinetics, 2013
Oculocutaneous albinism type 4: six novel mutations in the membrane-associated transporter protein gene and their phenotypes.
Inagaki K et al.
Pigment Cell Research, 2006
Oculocutaneous albinism type 4 is one of the most common types of albinism in Japan.
Inagaki K et al.
American Journal of Human Genetics, 2004
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