Mutations in ZASP define a novel form of muscular dystrophy in humans

Annals of Neurology

Volumn 57, Issue 2, 2005, Pages 269-276

  Selcen, Duygu ^a   Engel, Andrew G ^a  

^a MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MEMBRANE PROTEIN; PROTEIN ZASP; UNCLASSIFIED DRUG;

ADULT; AGED; ARTICLE; CONTROLLED STUDY; DOMINANT INHERITANCE; EXON; FEMALE; GENE MUTATION; GENETIC LINKAGE; HEART DISEASE; HETEROZYGOSITY; HUMAN; MALE; MISSENSE MUTATION; MUSCLE WEAKNESS; MUSCULAR DYSTROPHY; PERIPHERAL NEUROPATHY; PRIORITY JOURNAL; PROTEIN MOTIF; STEREOTYPY;

ADAPTOR PROTEINS, SIGNAL TRANSDUCING; ADULT; AGED; AMINO ACID SEQUENCE; BASE SEQUENCE; CARRIER PROTEINS; DNA MUTATIONAL ANALYSIS; FEMALE; HOMEODOMAIN PROTEINS; HUMANS; IMMUNOHISTOCHEMISTRY; MALE; MICROSCOPY, ELECTRON, TRANSMISSION; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUSCLE, SKELETAL; MUSCULAR DYSTROPHIES; MUTATION; POLYMERASE CHAIN REACTION;

EID: 13144260646     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.20376     Document Type: Article

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