Phenotypic variability leads to under-recognition of HNPP

Journal of Clinical Neuromuscular Disease

Volumn 3, Issue 3, 2002, Pages 106-112

  Kumar, Neeraj ^a   Muley, Suraj ^a   Pakiam, Anthony ^a   Parry, Gareth J ^a,b  

^a UNIVERSITY OF MINNESOTA   (United States)

^b AUCKLAND CITY HOSPITAL   (New Zealand)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; BRACHIAL PLEXUS; CHILD; CHROMOSOME 17; CHROMOSOME DELETION; CLINICAL ARTICLE; CLINICAL EXAMINATION; CONTROLLED STUDY; DIAGNOSTIC ERROR; FAMILY HISTORY; FEMALE; GENETIC IDENTIFICATION; GENETIC PROCEDURES; HEREDITARY MOTOR SENSORY NEUROPATHY; HIGH RISK POPULATION; HUMAN; HUMAN TISSUE; MALE; MONONEUROPATHY MULTIPLEX; NERVE BIOPSY; NERVE PARALYSIS; NERVOUS SYSTEM ELECTROPHYSIOLOGY; NEUROPATHY; PERIPHERAL NEUROPATHY; PHENOTYPIC VARIATION; PRIORITY JOURNAL; QUESTIONNAIRE; SURAL NERVE; SYMPTOMATOLOGY; TELEPHONE;

EID: 0036198868     PISSN: 15220443     EISSN: None     Source Type: Journal    
DOI: 10.1097/00131402-200203000-00002     Document Type: Article

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