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Article

P gene mutations in patients with oculocutaneous albinism and findings suggestive of Hermansky-Pudlak syndrome.

Journal of medical genetics - 1 Jun 2004

Garrison N A, Yi Z, Cohen-Barak O, Huizing M, Hartnell L M, Gahl W A, Brilliant M H

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Share to Albinism, Oculocutaneous
Share to Alleles
Share to Child, Preschool
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Hermanski-Pudlak Syndrome

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Share to Monophenol Monooxygenase

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Identifiers

PMID: 15173252
DOI: 10.1136/jmg.2003.014902
PMCID: PMC1735794

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P gene mutations in patients with oculocutaneous albinism and findings suggestive of Hermansky-Pudlak syndrome.PMID 15173252Read ↗

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