Genotype/phenotype correlations in x-linked dominant charcot-marie-tooth disease

Annals of the New York Academy of Sciences

Volumn 883, Issue , 1999, Pages 366-382

  Hahn, Angelika F ^a,c   Bolton, Charles F ^a   White, Christopher M ^d   Brown, William F ^b   Tuuha, Sascha E ^a   Tan, Charles C ^a   Ainsworth, Peter J ^a  

^a UNIVERSITY OF WESTERN ONTARIO   (Canada)

^b TUFTS MEDICAL CENTER   (United States)

^c LONDON HEALTH SCIENCES CENTRE   (Canada)

^d London Health Sciences Centre ^*

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 32; GAP JUNCTION PROTEIN;

ARTICLE; CHROMOSOME MAP; DOMINANT GENE; FEMALE; GENETICS; GENOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MIDDLE AGED; MUTATION; NERVE CONDUCTION; PATHOLOGY; PATHOPHYSIOLOGY; PEDIGREE; PERIPHERAL NERVE; PHENOTYPE; SEXUAL DEVELOPMENT; X CHROMOSOME;

CHARCOT-MARIE-TOOTH DISEASE; CHROMOSOME MAPPING; CONNEXINS; FEMALE; GENES, DOMINANT; GENOTYPE; HUMANS; MALE; MIDDLE AGED; MUTATION; NEURAL CONDUCTION; PEDIGREE; PERIPHERAL NERVES; PHENOTYPE; SEX CHARACTERISTICS; X CHROMOSOME;

EID: 0033554328     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.1999.tb08598.x     Document Type: Article

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