Familial hemiplegic migraine in the west of Scotland: A clinical and genetic study of seven families

Journal of Neurology Neurosurgery and Psychiatry

Volumn 61, Issue 6, 1996, Pages 616-620

  Ahmed, M A S ^a   Reid, Evan ^b,c,d   Cooke, A ^b   Arngrímsson, Reynir ^b   Tolmie, J L ^b   Stephenson, J B P ^a  

^a ROYAL HOSPITAL FOR SICK CHILDREN   (United Kingdom)

^b UNIVERSITY OF GLASGOW   (United Kingdom)

^c UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^d CAMBRIDGE UNIVERSITY HOSPITALS NHS FOUNDATION TRUST   (United Kingdom)

Author keywords

Chromosome 19p; Familial hemiplegic migraine; Genetics

Indexed keywords

ARTICLE; CHROMOSOME 19P; CLINICAL ARTICLE; CLINICAL FEATURE; DISEASE SEVERITY; FAMILIAL DISEASE; FAMILY STUDY; FEMALE; GENETIC HETEROGENEITY; GENETIC LINKAGE; HEMIPLEGIA; HUMAN; MALE; MIGRAINE; PRIORITY JOURNAL; UNITED KINGDOM;

EID: 0030452116     PISSN: 00223050     EISSN: None     Source Type: Journal    
DOI: 10.1136/jnnp.61.6.616     Document Type: Article

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