Characteristics of clinical and electrophysiological pattern of Charcot-Marie-Tooth 4C

Journal of the Peripheral Nervous System

Volumn 17, Issue 1, 2012, Pages 112-122

  Yger, Marion ^a   Stojkovic, Tanya ^a   Tardieu, Sandrine ^b,c   Maisonobe, Thierry ^b   Brice, Alexis ^b,c   Echaniz Laguna, Andoni ^d   Alembik, Yves ^d   Girard, Samantha ^b   Cazeneuve, Cécile ^b,c   LeGuern, Eric ^b,c   Dubourg, Odile ^a  

^a ASSISTANCE PUBLIQUE HÔPITAUX DE PARIS   (France)

^b PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^c SORBONNE UNIVERSITÉ   (France)

^d UNIVERSITY HOSPITAL OF STRASBOURG   (France)

Author keywords

Charcot Marie Tooth disease; Demyelinating disease; SH3TC2; Type 4C

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CHARCOT MARIE TOOTH 4C; CLINICAL ARTICLE; CLINICAL FEATURE; CRANIAL NERVE; ELECTROPHYSIOLOGY; FAMILY HISTORY; FEMALE; GENE; GENE MUTATION; GENE SEQUENCE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MOLECULAR DIAGNOSIS; MOLECULAR GENETICS; PRIORITY JOURNAL; SCOLIOSIS; SH3TC2 GENE;

ADULT; CHARCOT-MARIE-TOOTH DISEASE; ELECTROPHYSIOLOGY; FEMALE; HUMANS; MALE; MIDDLE AGED; MUTATION; POLYMERASE CHAIN REACTION; PROTEINS; YOUNG ADULT;

EID: 84859406203     PISSN: 10859489     EISSN: 15298027     Source Type: Journal    
DOI: 10.1111/j.1529-8027.2012.00382.x     Document Type: Article

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