Erratum: Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1) (Journal of Clinical Investigation (2005) 112 (450-456) DOI:10.1172/JCI200318264);Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)

Journal of Clinical Investigation

Volumn 112, Issue 3, 2003, Pages 450-456

  Ménasché, Gaël ^a   Ho, Chen Hsuan ^a   Sanal, Ozden ^b   Feldmann, Jérôme ^a   Tezcan, Ilhan ^b   Ersoy, Fügen ^b   Houdusse, Anne ^c   Fischer, Alain ^a   De Saint Basile, Geneviève ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

^b HACETTEPE UNIVERSITY   (Turkey)

^c INSTITUT CURIE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

GUANOSINE TRIPHOSPHATASE; MELANOPHILIN; MYOSIN V; MYOSIN VA; PROTEIN; RAB27 PROTEIN; UNCLASSIFIED DRUG; CARRIER PROTEIN; DNA; MLPH PROTEIN, HUMAN; MLPH PROTEIN, MOUSE; MYO5A PROTEIN, HUMAN; MYO5A PROTEIN, MOUSE; MYOSIN HEAVY CHAIN; RAB PROTEIN; RAB27A PROTEIN, HUMAN; RAB27A PROTEIN, MOUSE; SIGNAL TRANSDUCING ADAPTOR PROTEIN;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CONTROLLED STUDY; DISEASE ASSOCIATION; DISEASE CLASSIFICATION; DISEASE SEVERITY; EXOCYTOSIS; EXON; GENE DELETION; GENE MUTATION; GENETIC CODE; GENETIC VARIABILITY; GRISCELLI SYNDROME; HAIR; HUMAN; HUMAN CELL; HUMAN TISSUE; HYPOPIGMENTATION; IMMUNOCOMPETENT CELL; IMMUNOPATHOGENESIS; MELANOCYTE; NERVE CELL; NEUROLOGIC DISEASE; NUCLEOTIDE SEQUENCE; ORTHOLOGY; PHENOTYPE; PRIORITY JOURNAL; SECRETORY GRANULE; AMINO ACID SEQUENCE; ANIMAL; BIOLOGICAL MODEL; FEMALE; GENETICS; MALE; MELANOSOME; METABOLISM; MISSENSE MUTATION; MOLECULAR GENETICS; MOUSE; MUTATION; PATHOLOGY; PEDIGREE; SYNDROME;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CARRIER PROTEINS; DNA; EXONS; FEMALE; HAIR; HUMANS; HYPOPIGMENTATION; MALE; MELANOSOMES; MICE; MODELS, BIOLOGICAL; MOLECULAR SEQUENCE DATA; MUTATION; MUTATION, MISSENSE; MYOSIN HEAVY CHAINS; MYOSIN TYPE V; PEDIGREE; PHENOTYPE; RAB GTP-BINDING PROTEINS; SEQUENCE DELETION; SYNDROME;

EID: 0042388106     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/JCI200518264C1     Document Type: Erratum

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