메뉴 건너뛰기




Volumn 68, Issue 6, 2001, Pages 1521-1526

Benign familial infantile convulsions: Mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity

(22)  Malacarne, Michela a   Gennaro, Elena a   Madia, Francesca a   Pozzi, Sarah b   Vacca, Daniela c   Barone, Baldassare d,e   Dalla Bernardina, Bernardo d,f   Bianchi, Amedeo a,d   Bonanni, Paolo d,g,h   De Marco, Pasquale d,i   Gambardella, Antonio d,j   Giordano, Lucio d,k   Lispi, Maria Luisa d,l   Romeo, Antonino d,m   Santorum, Enrica d,f,n   Vanadia, Francesca d,o   Vecchi, Marilena d,p   Veggiotti, Pierangelo d   Vigevano, Federico d,l   Viri, Franco d,m   more..


Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; BENIGN CHILDHOOD EPILEPSY; CHROMOSOME 19Q; CHROMOSOME 2Q; CHROMOSOME MAP; CLINICAL ARTICLE; FAMILY; FOUNDER EFFECT; GENE CLUSTER; GENE LOCUS; GENETIC HETEROGENEITY; HUMAN; IDIOPATHIC DISEASE; ITALY; PRIORITY JOURNAL;

EID: 0034987775     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/320596     Document Type: Article
Times cited : (70)

References (23)
  • 12
    • 0033039497 scopus 로고    scopus 로고
    • Prospects for whole-genome linkage disequilibrium mapping of common disease genes
    • (1999) Nat Genet , vol.22 , pp. 139-144
    • Kruglyak, L.1
  • 15
    • 0033858589 scopus 로고    scopus 로고
    • Study of the voltagegated sodium channel beta 1 subunit gene (SCN1B) in the benign familial infantile convulsions syndrome (BFIC)
    • (2000) Hum Mut , vol.16 , pp. 139-142
    • Moulard, B.1    Buresi, C.2    Malafosse, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.