PRRT2 mutations: Exploring the phenotypical boundaries

Journal of Neurology, Neurosurgery and Psychiatry

Volumn 85, Issue 4, 2014, Pages 462-465

  Djémié, Tania ^a,b   Weckhuysen, Sarah ^a,b,c   Holmgren, Philip ^a,b   Hardies, Katia ^a,b   Van Dyck, Tine ^a,b   Hendrickx, Rik ^a,b   Schoonjans, An Sofie ^d   Van Paesschen, Wim ^e   Jansen, Anna C ^f,g   De Meirleir, Linda ^f   Selim, Laila Abdel Moteleb ^h   Girgis, Marian Y ^h   Buyse, Gunnar ^e   Lagae, Lieven ^e   Smets, Katrien ^a,b,d   Smouts, Iris ^a,b,d   Claeys, Kristl G ⁱ   Van Den Bergh, Vic ^j   Grisar, Thierry ^k   Blatt, Ilan ^l   Shorer, Zamir ^m   Roelens, Filip ⁿ   Afawi, Zaid ^m   Helbig, Ingo ^o   Ceulemans, Berten ^d,p   De Jonghe, Peter ^a,b,d   Suls, Arvid ^a,b   more..

^a UNIVERSITY OF ANTWERP   (Belgium)

^b UNIVERSITY OF ANTWERP   (Belgium)

^c EPILEPSY CENTER KEMPENHAEGHE   (Netherlands)

^d ANTWERP UNIVERSITY HOSPITAL   (Belgium)

^e UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^f UNIVERSITY HOSPITAL BRUSSELS   (Belgium)

^g VRIJE UNIVERSITEIT BRUSSEL   (Belgium)

^h CAIRO UNIVERSITY   (Egypt)

ⁱ UNIVERSITY HOSPITAL RWTH AACHEN   (Germany)

^j Hospital of Turnhout   (Belgium)

^k UNIVERSITY OF LIÈGE   (Belgium)

^l SHEBA MEDICAL CENTER   (Israel)

^m BEN GURION UNIVERSITY OF THE NEGEV   (Israel)

ⁿ Heilig Hart Ziekenhuis   (Belgium)

^o UNIVERSITY OF KIEL   (Germany)

^p Epilepsy Center for Children and Youth   (Belgium)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BENIGN FAMILIAL INFANTILE CONVULSION; CHOREOATHETOSIS; CLINICAL FEATURE; CONTROLLED STUDY; CONVULSION; DYSKINESIA; FEBRILE CONVULSION; GENE; HETEROZYGOSITY; HUMAN; INFANTILE CONVULSIONS WITH CHOREOATHETOSIS; LEARNING DISORDER; LENNOX GASTAUT SYNDROME; MAJOR CLINICAL STUDY; MUTATIONAL ANALYSIS; PAROXYSMAL DYSKINESIA; PRIORITY JOURNAL; PRRT2 GENE; SEQUENCE ANALYSIS;

CLINICAL NEUROLOGY; EPILEPSY; GENETICS; NEUROGENETICS;

EPILEPSY; FEMALE; HUMANS; LEARNING DISORDERS; MALE; MEMBRANE PROTEINS; MOTOR SKILLS DISORDERS; NERVE TISSUE PROTEINS; PEDIGREE; PHENOTYPE; POINT MUTATION;

EID: 84895813214     PISSN: 00223050     EISSN: 1468330X     Source Type: Journal    
DOI: 10.1136/jnnp-2013-305122     Document Type: Article

References (13)

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