SCOPUS 정보 검색 플랫폼

Current Molecular Medicine

Volumn 2, Issue 5, 2002, Pages 451-467

Disorders of vesicles of lysosomal lineage: The Hermansky-Pudlak syndromes

(2) Huizing, M a Gahl, W A a

a EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH AND HUMAN DEVELOPMENT (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADAPTOR PROTEIN 3 COMPLEX; ADENINE; COAT PROTEIN; CYTOPLASM PROTEIN; GUANINE; PROTEIN SUBUNIT; UNCLASSIFIED DRUG; CARRIER PROTEIN; HPS1 PROTEIN, HUMAN; HPS1 PROTEIN, MOUSE; HPS3 PROTEIN, HUMAN; MEMBRANE PROTEIN;

BLEEDING; CELL COMPARTMENTALIZATION; CELL VACUOLE; CHILDHOOD DISEASE; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE SEVERITY; DROSOPHILA; ELECTRON MICROSCOPY; ENDOSOME; EXON; FATALITY; GENE DELETION; GENE DUPLICATION; GENE IDENTIFICATION; GENE MUTATION; GENETIC CODE; GENETIC DISORDER; HOMOZYGOTE; HUMAN; HYPOPIGMENTATION; INFECTION; JEW; LUNG FIBROSIS; LYSOSOME; MELANOSOME; MOLECULAR GENETICS; MOUSE; NEUTROPENIA; NONHUMAN; OCULAR ALBINISM; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN PROCESSING; PUERTO RICO; REVIEW; THROMBOCYTE; ANIMAL; DISEASE MODEL; FIBROBLAST; GENETICS; METABOLISM; MUTATION; PATHOLOGY;

ANIMAL; CARRIER PROTEINS; DISEASE MODELS, ANIMAL; EXONS; FIBROBLASTS; HERMANSKI-PUDLAK SYNDROME; HUMAN; MEMBRANE PROTEINS; MICE; MUTATION; ANIMALS; HUMANS;

EID: 0035990977 PISSN: 15665240 EISSN: None Source Type: Journal
DOI: 10.2174/1566524023362357 Document Type: Review

Times cited : (106)

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