Clinical and electrophysiologic features of HNPP patients with 17p11.2 deletion

Acta Neurologica Scandinavica

Volumn 108, Issue 5, 2003, Pages 352-358

  Hong, Y H ^a   Kim, M ^a   Kim, H J ^a   Sung, J J ^a   Kim, S H ^a   Lee, K W ^a  

^a Seoul National University Hospital   (South Korea)

Author keywords

Charcot Marie Tooth disease type IA (CMT1A); Hereditary neuropathy with liability to pressure palsies (HNPP); Polymerase chain reaction (PCR); Polyneuropathy

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME 17P; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE SEVERITY; ELECTROPHYSIOLOGY; FEMALE; HEREDITARY MOTOR SENSORY NEUROPATHY; HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES; HUMAN; LATENT PERIOD; MALE; MOTOR NERVE CONDUCTION; NERVE COMPRESSION; PERIPHERAL NEUROPATHY; PERONEUS NERVE; POLYNEUROPATHY; PROGNOSIS; SENSORY NERVE CONDUCTION; ULNAR NERVE;

ADOLESCENT; ADULT; CHARCOT-MARIE-TOOTH DISEASE; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 17; DIAGNOSIS, DIFFERENTIAL; ELECTRODIAGNOSIS; FEMALE; GENE DELETION; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HUMANS; MALE; MIDDLE AGED; NEURAL CONDUCTION; POLYMERASE CHAIN REACTION;

EID: 0242320245     PISSN: 00016314     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1600-0404.2003.00132.x     Document Type: Article

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