Axonal phenotype of Charcot-Marie-Tooth disease associated with a mutation in the myelin protein zero gene

Journal of Neurology Neurosurgery and Psychiatry

Volumn 66, Issue 6, 1999, Pages 779-782

  Chapon, F ^a,b   Latour, P ^c   Diraison, P ^b   Schaeffer, S ^b   Vandenberghe, A ^c  

^a Center de Neuropathologie   (France)

^b CAEN UNIVERSITY HOSPITAL   (France)

^c Hopital de l'Antiquaille   (France)

Author keywords

Argyll Robertson syndrome; Axonal neuropathy; Charcot Marie Tooth; Myelin protein zero

Indexed keywords

METHIONINE; MYELIN PROTEIN; THREONINE;

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; DYSPHAGIA; ELECTROPHYSIOLOGY; FEMALE; GENE MUTATION; HEARING IMPAIRMENT; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; NERVE BIOPSY; NERVE FIBER; PERIPHERAL NEUROPATHY; PHENOTYPE; PRIORITY JOURNAL; PUPIL DISEASE; SEQUENCE ANALYSIS;

EID: 0033027371     PISSN: 00223050     EISSN: None     Source Type: Journal    
DOI: 10.1136/jnnp.66.6.779     Document Type: Article

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