Tomaculous neuropathy: A clinical and electrophysiological study in patients with and without 1.5-Mb deletions in chromosome 17p11.2

Muscle and Nerve

Volumn 19, Issue 1, 1996, Pages 16-22

  Amato, Anthony A ^a,d   Gronseth, Gary S ^a   Callerame, Kevin J ^a   Kagan Hallet, Kathleen S ^b   Bryan, Wilson W ^c   Barohn, Richard J ^c  

^a WILFORD HALL MEDICAL CENTER   (United States)

^b UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER AT SAN ANTONIO   (United States)

^c UNIVERSITY OF TEXAS AT DALLAS   (United States)

^d 59th Med Wg/PSMN   (United States)

Author keywords

hereditary neuropathy with liability to pressure palsies; mutations; peripheral myelin protein 22; tomaculous neuropathy

Indexed keywords

MYELIN PROTEIN;

ADOLESCENT; ADULT; AGED; ARTICLE; CHROMOSOME 17P; CHROMOSOME DELETION; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; FEMALE; HUMAN; HUMAN TISSUE; MALE; NERVE CONDUCTION; NEUROPATHY; PRIORITY JOURNAL; SCHOOL CHILD;

ADOLESCENT; ADULT; CHILD; CHROMOSOMES, HUMAN, PAIR 17; DNA; ELECTROPHYSIOLOGY; FEMALE; GENE DELETION; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HUMANS; MALE; MIDDLE AGED; NEUROLOGIC EXAMINATION; RETROSPECTIVE STUDIES;

EID: 0030031715     PISSN: 0148639X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-4598(199601)19:1<16::AID-MUS3>3.0.CO;2-B     Document Type: Article

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