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- [42] Tyrosinase gene mutations in oculocutaneous albinism 1 (OCA1): definition of the phenotype Human Genetics, 2003, 113 : 502 - 513
- [48] Angelman syndrome associated with oculocutaneous albinism due to an intragenic deletion of the P gene AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2003, 119A (02): : 180 - 183