Oculocutaneous albinism type 2 with a P gene missense mutation in a patient with Angelman syndrome
- PMID: 10905897
- PMCID: PMC1734585
- DOI: 10.1136/jmg.37.5.392
Oculocutaneous albinism type 2 with a P gene missense mutation in a patient with Angelman syndrome
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