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Neurological Sciences

Volumn 32, Issue SUPPL. 1, 2011, Pages

The genetic features of 24 patients affected by familial and sporadic hemiplegic migraine

(7) Gallanti, A a Cardin, V b Tonelli, A c Bussone, G d Bresolin, N a,b Mariani, C b,e Bassi, M T c

a FONDAZIONE IRCCS CA GRANDA OSPEDALE MAGGIORE POLICLINICO (Italy)

b UNIVERSITY OF MILAN (Italy)

c SCIENTIFIC INSTITUTE (Italy)

d DEPARTMENT OF NEUROSURGERY (Italy)

e UNIVERSITY OF MILAN (Italy)

Author keywords

ATP1A2; FHM; SHM

Indexed keywords

BRAIN PROTEIN; PROTEIN ATP1A2; PROTEIN CACNA1A; PROTEIN FHM1; PROTEIN FHM2; PROTEIN FHM3; SODIUM CHANNEL NAV1.1; UNCLASSIFIED DRUG;

ADULT; ARTICLE; ATP1A2 GENE; CACNA1A GENE; CLINICAL ARTICLE; DNA SCREENING; FAMILIAL HEMIPLEGIC MIGRAINE; FEMALE; FHM1 GENE; FHM2 GENE; FHM3 GENE; GENE MUTATION; GENETIC ANALYSIS; HUMAN; MALE; MIGRAINE WITH AURA; PATHOPHYSIOLOGY; SCN1A GENE; SPORADIC HEMIPLEGIC MIGRAINE;

ADULT; CHILD; DNA MUTATIONAL ANALYSIS; FEMALE; GENOTYPE; HUMANS; MALE; MIDDLE AGED; MIGRAINE WITH AURA; MUTATION; SODIUM-POTASSIUM-EXCHANGING ATPASE;

EID: 79960115251 PISSN: 15901874 EISSN: 15903478 Source Type: Journal
DOI: 10.1007/s10072-011-0517-4 Document Type: Article

Times cited : (14)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.