Hereditary motor and sensory neuropathy-Lom (HMSNL) in a Spanish family: Clinical, electrophysiological, pathological and genetic studies

Neuromuscular Disorders

Volumn 10, Issue 8, 2000, Pages 578-583

  Colomer, J ^a   Iturriaga, C ^a   Kalaydjieva, L ^b,c   Angelicheva, D ^b   King, R H M ^d   Thomas, P K ^d  

^a HOSPITAL SANT JOAN DE DÉU   (Spain)

^b EDITH COWAN UNIVERSITY   (Australia)

^c UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^d ROYAL FREE HOSPITAL   (United Kingdom)

Author keywords

Deafness; Hereditary motor and sensory neuropathy type Lom

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CASE REPORT; CLINICAL EXAMINATION; CLINICAL FEATURE; CONSANGUINITY; ELECTROPHYSIOLOGY; EVOKED AUDITORY RESPONSE; FEMALE; GENETIC ANALYSIS; GENETIC LINKAGE; HAPLOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; NERVE BIOPSY; NERVE CONDUCTION; NEUROPATHOLOGY; NEUROPHYSIOLOGY; PERCEPTION DEAFNESS; PRIORITY JOURNAL; SCHWANN CELL; SPAIN; SURAL NERVE;

ADOLESCENT; ADULT; ATROPHY; BIOPSY; CASE REPORT; ELECTROMYOGRAPHY; EVOKED POTENTIALS, AUDITORY, BRAIN STEM; FEMALE; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HUMAN; MALE; MUSCLE, SKELETAL; NEURAL CONDUCTION; PERIPHERAL NERVES; SPAIN;

EID: 0033784885     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-8966(00)00149-8     Document Type: Article

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