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Volumn 27, Issue 1, 2002, Pages 49-52
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A novel chronic childhood sensory predominant neuropathy
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Author keywords
[No Author keywords available]
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Indexed keywords
AREFLEXIA;
ARTICLE;
AUTOSOMAL RECESSIVE INHERITANCE;
CASE REPORT;
CHILDHOOD;
CONSANGUINITY;
ELECTROMYOGRAPHY;
ETHNIC GROUP;
FACE DYSMORPHIA;
FEMALE;
GROWTH RETARDATION;
HUMAN;
INFANT;
MALE;
MOSLEM;
MUSCLE HYPOTONIA;
NERVE BIOPSY;
NERVE CONDUCTION;
NEUROPATHY;
PERCEPTION DEAFNESS;
PHENOTYPE;
PRESCHOOL CHILD;
PRIORITY JOURNAL;
SENSORY DYSFUNCTION;
SURAL NERVE;
ARABS;
CHILD, PRESCHOOL;
FAMILY HEALTH;
FEMALE;
HEREDITARY MOTOR AND SENSORY NEUROPATHIES;
HUMANS;
INFANT;
MALE;
NEURAL CONDUCTION;
NEURONS, AFFERENT;
PEDIGREE;
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EID: 0036325278
PISSN: 08878994
EISSN: None
Source Type: Journal
DOI: 10.1016/S0887-8994(02)00376-4 Document Type: Article |
Times cited : (6)
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References (18)
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