Tomaculous neuropathy in Charcot-Marie-Tooth disease with myelin protein zero gene mutation

Journal of the Neurological Sciences

Volumn 153, Issue 1, 1997, Pages 106-109

  Tachi, Nobutada ^a   Kozuka, Naoki ^a   Ohya, Kazuhiro ^b   Chiba, Shunzo ^b   Sasaki, Kimio ^c  

^a SAPPORO MEDICAL UNIVERSITY   (Japan)

^b SAPPORO MEDICAL UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c NONE

Author keywords

Mutation of the Po gene; Tomaculous neuropathy

Indexed keywords

MYELIN PROTEIN;

ARTICLE; CASE REPORT; CHILD; FEMALE; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN TISSUE; NERVE BIOPSY; NEUROPATHY; PHENOTYPE; PRIORITY JOURNAL; SURAL NERVE;

AMINO ACID SUBSTITUTION; CHARCOT-MARIE-TOOTH DISEASE; CHILD; DNA; FEMALE; HUMANS; MYELIN PROTEINS; PERIPHERAL NERVES; SURAL NERVE;

EID: 0031443763     PISSN: 0022510X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-510X(97)00202-5     Document Type: Article

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