Clinical, genetic and electrophysiologic correlation in hereditary neuropathy with liability to pressure palsies with involvement of PMP22 gene at chromosome 17p11.2

European Journal of Neurology

Volumn 4, Issue 3, 1997, Pages 274-286

  Cruz Martinez A ^a,e   Bort, S ^b   Arpa, J ^c   Duarte, J ^d   Palau, F ^b  

^a Hospital La Luz   (Spain)

^b HOSPITAL UNIVERSITARIO LA FE   (Spain)

^c HOSPITAL UNIVERSITARIO LA PAZ   (Spain)

^d HOSPITAL GENERAL DE SEGOVIA   (Spain)

^e NONE   (Spain)

Author keywords

CMT1A HNPP locus 1.5 Mb deletion; Conduction block in HNPP; DNA analysis; Electrophysiology; HNPP; Point mutation in PMP22 gene; Susceptibility to pressure palsies

Indexed keywords

MYELIN PROTEIN;

ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BRACHIAL PLEXUS; CHROMOSOME 17P; CLINICAL ARTICLE; CLINICAL EXAMINATION; CONTROLLED STUDY; ELECTROPHYSIOLOGY; FAMILY; FEMALE; GENE LOCUS; GENE MUTATION; HUMAN; INTRON; MALE; NERVE BLOCK; NEUROPATHY; PARALYSIS; POINT MUTATION; PRIORITY JOURNAL;

EID: 0030791245     PISSN: 13515101     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1468-1331.1997.tb00347.x     Document Type: Article

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