Hereditary recurrent focal neuropathies: Clinical and molecular features

Neurology

Volumn 54, Issue 3, 2000, Pages 546-551

  Stögbauer, Florian ^a   Young, P ^a   Kuhlenbaumer G ^a,b   De Jonghe, P ^b,c   Timmerman, V ^b  

^a UNIVERSITY OF MÜNSTER   (Germany)

^b DEPARTMENT OF PLANT SYSTEMS BIOLOGY   (Belgium)

^c ANTWERP UNIVERSITY HOSPITAL   (Belgium)

Author keywords

Brachial neuritis; Hereditary neuralgic amyotrophy; Hereditary neuropathy with liability to pressure palsies; Peripheral myelin protein 22

Indexed keywords

GENE PRODUCT; PERIPHERAL MYELIN PROTEIN 22; UNCLASSIFIED DRUG;

ALLELE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 17P; CHROMOSOME 17Q; CLINICAL FEATURE; GENE MUTATION; HEREDITARY NEURALGIC AMYOTROPHY; HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSY; HUMAN; NEUROPATHY; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN EXPRESSION; RECURRENT DISEASE; REVIEW;

EID: 0343067099     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/wnl.54.3.546     Document Type: Review

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