Charcot-Marie-Tooth disease in Northern England

Journal of Neurology, Neurosurgery and Psychiatry

Volumn 83, Issue 5, 2012, Pages 572-573

  Foley, Charlotte ^a   Schofield, Ian ^b   Eglon, Gail ^a   Bailey, Geraldine ^a   Chinnery, Patrick F ^a   Horvath, Rita ^a  

^a NEWCASTLE UNIVERSITY   (United Kingdom)

^b NEWCASTLE UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL FEATURE; CMT1A GENE; DEMYELINATING DISEASE; FAMILY HISTORY; FEMALE; GENE; GENE DELETION; GENE DUPLICATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSY; HUMAN; LETTER; MAJOR CLINICAL STUDY; MALE; MOLECULAR GENETICS; MOTOR NERVE CONDUCTION; NERVOUS SYSTEM ELECTROPHYSIOLOGY; NEUROPATHY; PMP22 GENE; POPULATION RESEARCH; PREVALENCE; PRIORITY JOURNAL; SEX DIFFERENCE; UNITED KINGDOM;

EID: 84859718053     PISSN: 00223050     EISSN: 1468330X     Source Type: Journal    
DOI: 10.1136/jnnp-2011-300285     Document Type: Letter

References (5)

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5. Meretoja P, Silander K, Kalimo H, et al. Epidemiology of hereditary neuropathy with liability to pressure palsies (HNPP) in south western Finland. Neuromuscul Disord 1997;7:529-32. (Pubitemid 28008962)