X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: Clinical and electrophysiologic study

Neurology

Volumn 50, Issue 4, 1998, Pages 1074-1082

  Birouk, N ^a,c   LeGuern, E ^a   Maisonobe, T ^a   Rouger, H ^a   Gouider, R ^a   Tardieu, S ^a   Gugenheim, M ^a   Routon, M C ^b   Leger J M ^a   Agid, Y ^a   Brice, A ^a   Bouche, P ^a  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b HÔPITAL SAINT VINCENT DE PAUL   (France)

^c IBN SINA HOSPITAL   (Morocco)

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 32;

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CLINICAL ARTICLE; ELECTRON MICROSCOPY; FEMALE; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MICROSCOPY; MISSENSE MUTATION; MOTOR NERVE CONDUCTION; MUSCLE ACTION POTENTIAL; NONSENSE MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; SURAL NERVE; X CHROMOSOME LINKED DISORDER;

EID: 0031901040     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.50.4.1074     Document Type: Article

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