Deletions of chromosome 17p11.2 in multifocal neuropathies

Annals of Neurology

Volumn 39, Issue 2, 1996, Pages 180-186

  Tyson, J ^a   Malcolm, S ^a   Thomas, P K ^b,c   Harding, A E ^b  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c ROYAL FREE HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ACTION POTENTIAL; ADOLESCENT; ADULT; ARTICLE; CHROMOSOME 17P; CHROMOSOME DELETION; CLINICAL ARTICLE; CLINICAL FEATURE; DNA DETERMINATION; EVOKED MUSCLE RESPONSE; FEMALE; HEREDITARY SPINAL MUSCULAR ATROPHY; HUMAN; MALE; NERVE CONDUCTION; NEUROPATHY; PERIPHERAL NERVE; PRESCHOOL CHILD; PRIORITY JOURNAL;

ADOLESCENT; ADULT; CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; HUMANS; MALE; MIDDLE AGED; NERVE COMPRESSION SYNDROMES; NERVOUS SYSTEM; NERVOUS SYSTEM DISEASES;

EID: 0030048699     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410390207     Document Type: Article

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