Associated Papers
Novel compound heterozygous mutations in OCA2 gene were identified in a Chinese family with oculocutaneous albinism.
Jiang B et al.
Molecular Genetics & Genomic Medicine, 2024
37882226 (PubMed )
Supplement: MGG3-12-e2297-s002.xlsx › Supplementary_Table_2
Novel human pathological mutations. Gene symbol: OCA2. Disease: albinism, oculocutaneous II.
Ray K et al.
Human Genetics, 2010
Novel human pathological mutations. Gene symbol: OCA2. Disease: albinism, oculocutaneous II.
Ray K et al.
Human Genetics, 2010
Novel human pathological mutations. Gene symbol: OCA2. Disease: albinism, oculocutaneous II.
Renugadevi K et al.
Human Genetics, 2009
P gene mutations associated with oculocutaneous albinism type II (OCA2).
Oetting WS et al.
Human Mutation, 2005
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