Tyrosinase gene mutations in oculocutaneous albinism�1 (OCA1): definition of the phenotype
Year: 2003
Type: article
Study design: Observational Study
Source: Human Genetics
Institutions: University of Minnesota, Great Ormond Street Hospital
Language: English
Subfield: Cell Biology
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2051648246
