Mapping of Charcot-Marie-Tooth disease type 1C to chromosome 16p identifies a novel locus for demyelinating neuropathies

American Journal of Human Genetics

Volumn 70, Issue 1, 2002, Pages 244-250

  Street, Valerie A ^a   Goldy, Jeff D ^b   Golden, Alana S ^a   Tempel, Bruce L ^a   Bird, Thomas D ^a,c   Chance, Phillip F ^a,b  

^a UNIVERSITY OF WASHINGTON   (United States)

^b UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^c VA PUGET SOUND HEALTH CARE SYSTEM   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EPITHELIAL MEMBRANE PROTEIN 2; MEMBRANE PROTEIN; NUCLEOTIDE; UNCLASSIFIED DRUG;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 16P; CLINICAL FEATURE; DEMYELINATION; FEMALE; GENE LOCUS; GENE MUTATION; GENETIC LINKAGE; HAPLOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MARKER CHROMOSOME; MUSCLE ATROPHY; MUSCLE WEAKNESS; NERVE CONDUCTION; NUCLEOTIDE SEQUENCE; PEDIGREE; PRIORITY JOURNAL; SENSORY DYSFUNCTION; SEQUENCE ANALYSIS; SYMPTOM; TENDON REFLEX;

EID: 0036138107     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/337943     Document Type: Article

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