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Volumn 117, Issue 2, 1999, Pages 251-252
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Genetic defects and clinical characteristics of patients with a form of oculocutaneous albinism (Hermansky-Pudlak syndrome)
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Author keywords
[No Author keywords available]
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Indexed keywords
CLINICAL ARTICLE;
CLINICAL FEATURE;
CONTROLLED STUDY;
ENTERITIS;
GENE DUPLICATION;
GENETIC DISORDER;
HOMOZYGOSITY;
HUMAN;
LUNG FIBROSIS;
NYSTAGMUS;
OCULOCUTANEOUS ALBINISM;
PRIORITY JOURNAL;
PUERTO RICO;
SHORT SURVEY;
VISUAL ACUITY;
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EID: 0344573032
PISSN: 00039950
EISSN: None
Source Type: Journal
DOI: 10.1001/archopht.117.2.251 Document Type: Short Survey |
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Times cited : (2)
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References (1)
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