Phenotypic and genotypic heterogeneity in hereditary motor neuronopathy type V. A clinical, electrophysiological and genetic study

Brain

Volumn 123, Issue 8, 2000, Pages 1612-1623

  Auer Grumbach, Michaela ^a,c   Löscher, Wolfgang N ^a   Wagner, Klaus ^a   Petek, Erwin ^a   Körner, Eva ^a   Offenbacher, Hans ^b   Hartung, Hans Peter ^a  

^a UNIVERSITY OF GRAZ   (Austria)

^b GENERAL HOSPITAL KLAGENFURT   (Austria)

^c MEDICAL UNIVERSITY OF GRAZ   (Austria)

Author keywords

Charcot Marie Tooth; Chromosome 7p; Distal spinal muscular atrophy; Hereditary motor neuronopathy; HMN V

Indexed keywords

ADOLESCENT; ADULT; AGED; ANTERIOR HORN CELL DISEASE; ARTICLE; AUSTRIA; AUTOSOMAL DOMINANT DISORDER; BACK MUSCLE; CENTRAL NERVOUS SYSTEM; CHROMOSOME 7P; DIFFERENTIAL DIAGNOSIS; ELECTROMYOGRAPHY; ELECTROPHYSIOLOGY; FAMILIAL DISEASE; FEMALE; FOOT MALFORMATION; GAIT DISORDER; GENETIC HETEROGENEITY; GENETIC LINKAGE; HEREDITARY MOTOR SENSORY NEUROPATHY; HEREDITARY SPINAL MUSCULAR ATROPHY; HIGH RISK POPULATION; HUMAN; LATENT PERIOD; LEG MUSCLE; MAJOR CLINICAL STUDY; MALE; MOTOR DYSFUNCTION; MOTOR NERVE CONDUCTION; MOTOR NEUROPATHY; MUSCLE ACTION POTENTIAL; MUSCLE ATROPHY; MUSCLE TONE; ONSET AGE; PLANTARIS MUSCLE; PRIORITY JOURNAL; SCHOOL CHILD; SENSATION; TENDON REFLEX; THENAR;

EID: 0343090417     PISSN: 00068950     EISSN: None     Source Type: Journal    
DOI: 10.1093/brain/123.8.1612     Document Type: Article

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