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Volumn 31, Issue 10, 2010, Pages 1134-1141

High-throughput sequencing of a 4.1Mb linkage interval reveals FLVCR2 deletions and mutations in lethal cerebral vasculopathy

(32)  Thomas, Sophie a,b   Encha Razavi, Ferechté a,b   Devisme, Louise c   Etchevers, Heather a,b   Bessieres Grattagliano, Bettina d   Goudefroye, Géraldine a   Elkhartoufi, Nadia a   Pateau, Emilie e   Ichkou, Amale a   Bonnière, Maryse a,f   Marcorelle, Pascale g   Parent, Philippe g   Manouvrier, Sylvie h   Holder, Muriel h   Laquerrière, Annie i   Loeuillet, Laurence j   Roume, Joelle j   Martinovic, Jelena a   Mougou Zerelli, Soumaya a,b,k   Gonzales, Marie l   more..

e DIF   (France)

Author keywords

Arthrogryposis; Cerebral proliferative vasculopathy; Fetal lethality; FLVCR2; Fowler syndrome; Hydranencephaly

Indexed keywords

ALPHA SMOOTH MUSCLE ACTIN; CARRIER PROTEIN; FLVCR2 PROTEIN, HUMAN; VIRUS RECEPTOR;

EID: 79952198469     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.21329     Document Type: Article
Times cited : (24)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.