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Human Adenylate Kinase 2 Deficiency Causes a Profound Hematopoietic Defect Associated with Sensorineural Deafness
AuthID
P-00J-K4S
P-00J-K4S
22
Author(s)
Six, EM
·Picard, C
·Ditadi, A
·Chappedelaine, CD
·Morillon, E
·Valensi, F
·Simon-Stoos, KL
·[+2]·
Besse, C
·Wulffraat, NM
·Ferster, A
·Abecasis, MM
·Calvo, F
·Petit, C
·Candotti, F
·Abel, L
·Fischer, A
·Cavazzana-Calvo, M
Document Type
Article
Year published
2008
Published
in Nature Genetics - Nat Genet, ISSN: 1061-4036
Volume: 41, Issue: 1, Pages: 106-111
Indexing
Publication Identifiers
DOI: 10.1038/ng.278
Source Identifiers
ISSN: 1061-4036
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Name Order | Name | Name Order | Name | Name Order | Name | ||
---|---|---|---|---|---|---|---|
1 | Lagresle-Peyrou, C; | 2 | Six, EM; | 3 | Picard, C; | ||
4 | Rieux-Laucat, F; | 5 | Michel, V; | 6 | Ditadi, A; | ||
7 | Chappedelaine, CD; | 8 | Morillon, E; | 9 | Valensi, F; | ||
10 | Simon-Stoos, KL; | 11 | Mullikin, JC; | 12 | Noroski, LM; | ||
13 | Besse, C; | 14 | Wulffraat, NM; | 15 | Ferster, A; | ||
16 | Abecasis, MM; | 17 | Calvo, F; | 18 | Petit, C; | ||
19 | Candotti, F; | 20 | Abel, L; | 21 | Fischer, A; | ||
22 | Cavazzana-Calvo, M; |