Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: Clinical, electrophysiologic, and genetic aspects of a large family

Neurology

Volumn 46, Issue 5, 1996, Pages 1318-1324

  Quattrone, A ^a,f   Gambardella, A ^a   Bono, F ^a   Aguglia, U ^a   Bolino, A ^c   Bruni, A C ^d   Montesi, M P ^d   Oliveri, R L ^a   Sabatelli, M ^b   Tamburrini, O ^a   Valentino, P ^a   Van Broeckhoven, C ^e   Zappia, M ^a  

^a School of Medicine of Catanzaro   (Italy)

^b CATHOLIC UNIVERSITY   (Italy)

^c G GASLINI INSTITUTE   (Italy)

^d CNR   (Italy)

^e UNIVERSITY OF ANTWERP   (Belgium)

^f UNIVERSITY OF CHIETI   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CHROMOSOME 17P; CLINICAL ARTICLE; EVOKED AUDITORY RESPONSE; FEMALE; HEREDITARY MOTOR SENSORY NEUROPATHY; HISTOPATHOLOGY; HUMAN; HUMAN CELL; HUMAN TISSUE; MALE; MOLECULAR GENETICS; MOTOR NERVE CONDUCTION; MYELIN SHEATH; POINT MUTATION; PRESCHOOL CHILD; PRIORITY JOURNAL; SYMPTOMATOLOGY;

EID: 9344241377     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/wnl.46.5.1318     Document Type: Article

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