Autosomal recessive type II hereditary motor and sensory neuropathy with acrodystrophy

Journal of Neurology

Volumn 246, Issue 2, 1999, Pages 107-112

  Thomas, P K ^a   Claus, D ^b   King, R H M ^a  

^a ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL   (United Kingdom)

^b Neurologische Klinik   (Germany)

Author keywords

Autosomal recessive inheritance; Axonopathy; Hereditary motor and sensory neuropathy

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE CLASSIFICATION; ELECTROPHYSIOLOGY; FEMALE; HUMAN; HUMAN TISSUE; MALE; MOTOR NEUROPATHY; MUSCLE WEAKNESS; NERVE BIOPSY; PRIORITY JOURNAL; SENSORY NEUROPATHY; SIBLING;

ADULT; AGE OF ONSET; AGED; AXONS; CHILD; CONSANGUINITY; DISEASE PROGRESSION; ELECTROPHYSIOLOGY; FEMALE; FOOT DEFORMITIES, ACQUIRED; FOOT ULCER; GENES, RECESSIVE; GERMANY; HAND DEFORMITIES, ACQUIRED; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HUMANS; MALE; MIDDLE AGED; NEURAL CONDUCTION; PEDIGREE; TURKEY;

EID: 0033004883     PISSN: 03405354     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004150050316     Document Type: Article

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