• Citer

Phenotypical characterization of α-galactosidase A gene mutations identified in a large Fabry disease screening program in stroke in the young

par De Brabander, Isabel;De Deyn, Peter Paul;Sheorajpanday, Rishi;Ceuterick-De Groote, Chantal;Yperzeele, Laetitia;Brouns, Raf;Baker, Robert;Hughes, Derralynn;Belachew, Shibeshih;Sadzot, Bernard;Delbecq, Jean;De Keulenaer, Gilles;Dethy, Sophie ;Redondo Saez, Patricia;Eyskens, François;Fumal, Arnaud;Hemelsoet, Dimitri;Jeangette, Sandrine;Nuytten, Dirk;Sindic, Christian Jean Marie;Thijs, Vincent;Van Broeckhoven, Christine
Référence Clinical neurology and neurosurgery, 115, 7, page (1088-1093)
Publication Publié, 2013-07

Article révisé par les pairs

• Accès en ligne
• Détails
• Contenu
• Statistiques

Titre:	Phenotypical characterization of α-galactosidase A gene mutations identified in a large Fabry disease screening program in stroke in the young
Auteur:	De Brabander, Isabel; De Deyn, Peter Paul; Sheorajpanday, Rishi; Ceuterick-De Groote, Chantal; Yperzeele, Laetitia; Brouns, Raf; Baker, Robert; Hughes, Derralynn; Belachew, Shibeshih; Sadzot, Bernard; Delbecq, Jean; De Keulenaer, Gilles; Dethy, Sophie; Redondo Saez, Patricia; Eyskens, François; Fumal, Arnaud; Hemelsoet, Dimitri; Jeangette, Sandrine; Nuytten, Dirk; Sindic, Christian Jean Marie; Thijs, Vincent; Van Broeckhoven, Christine
Informations sur la publication:	Clinical neurology and neurosurgery, 115, 7, page (1088-1093)
Statut de publication:	Publié, 2013-07
Sujet CREF:	Chirurgie
	Neurologie
Mots-clés:	Cerebrovascular disease
	Fabry disease
	Family screening
	Genetics of stroke
	Phenotyping
	Risk factors for stroke
	Stroke in young
Note générale:	SCOPUS: ar.j
Langue:	Anglais
Identificateurs:	urn:issn:0303-8467
	info:doi/10.1016/j.clineuro.2012.11.003
	info:pii/S0303846712005719
	info:scp/84878851460
	info:pmid/23219219