Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness

C Lagresle-Peyrou; EM Six; C Picard; F Rieux-Laucat; V Michel; A Ditadi; C Demerens-de Chappedelaine; E Morillon; F. Valensi; KL Simon-Stoos; JC Mullikin; LM Noroski; C Besse; N.M. Wulffraat; A. Ferster; MM Abecasis; F Calvo; C Petit; F Candotti; L Abel; A. Fischer; M. Cavazzana-Calvo

Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness

Translated title of the contribution: Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness

C Lagresle-Peyrou, EM Six, C Picard, F Rieux-Laucat, V Michel, A Ditadi, C Demerens-de Chappedelaine, E Morillon, F. Valensi, KL Simon-Stoos, JC Mullikin, LM Noroski, C Besse, N.M. Wulffraat, A. Ferster, MM Abecasis, F Calvo, C Petit, F Candotti, L AbelA. Fischer, M. Cavazzana-Calvo

Research output: Contribution to journal › Article › Academic › peer-review

Translated title of the contribution	Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness
Original language	Undefined/Unknown
Pages (from-to)	106-111
Number of pages	6
Journal	Nature Genetics
Volume	41
Issue number	1
Publication status	Published - 2009

Cite this

Lagresle-Peyrou, C., Six, EM., Picard, C., Rieux-Laucat, F., Michel, V., Ditadi, A., Demerens-de Chappedelaine, C., Morillon, E., Valensi, F., Simon-Stoos, KL., Mullikin, JC., Noroski, LM., Besse, C., Wulffraat, N. M., Ferster, A., Abecasis, MM., Calvo, F., Petit, C., Candotti, F., ... Cavazzana-Calvo, M. (2009). Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness. Nature Genetics, 41(1), 106-111.

@article{c6aee60ef9cb4a7ab30e5bfdcb6aa36c,

title = "Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness",

author = "C Lagresle-Peyrou and EM Six and C Picard and F Rieux-Laucat and V Michel and A Ditadi and {Demerens-de Chappedelaine}, C and E Morillon and F. Valensi and KL Simon-Stoos and JC Mullikin and LM Noroski and C Besse and N.M. Wulffraat and A. Ferster and MM Abecasis and F Calvo and C Petit and F Candotti and L Abel and A. Fischer and M. Cavazzana-Calvo",

year = "2009",

language = "Undefined/Unknown",

volume = "41",

pages = "106--111",

journal = "Nature Genetics",

issn = "1061-4036",

publisher = "Nature Research",

number = "1",

}

Lagresle-Peyrou, C, Six, EM, Picard, C, Rieux-Laucat, F, Michel, V, Ditadi, A, Demerens-de Chappedelaine, C, Morillon, E, Valensi, F, Simon-Stoos, KL, Mullikin, JC, Noroski, LM, Besse, C, Wulffraat, NM, Ferster, A, Abecasis, MM, Calvo, F, Petit, C, Candotti, F, Abel, L, Fischer, A & Cavazzana-Calvo, M 2009, 'Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness', Nature Genetics, vol. 41, no. 1, pp. 106-111.

TY - JOUR

T1 - Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness

AU - Lagresle-Peyrou, C

AU - Six, EM

AU - Picard, C

AU - Rieux-Laucat, F

AU - Michel, V

AU - Ditadi, A

AU - Demerens-de Chappedelaine, C

AU - Morillon, E

AU - Valensi, F.

AU - Simon-Stoos, KL

AU - Mullikin, JC

AU - Noroski, LM

AU - Besse, C

AU - Wulffraat, N.M.

AU - Ferster, A.

AU - Abecasis, MM

AU - Calvo, F

AU - Petit, C

AU - Candotti, F

AU - Abel, L

AU - Fischer, A.

AU - Cavazzana-Calvo, M.

PY - 2009

Y1 - 2009

M3 - Article

SN - 1061-4036

VL - 41

SP - 106

EP - 111

JO - Nature Genetics

JF - Nature Genetics

IS - 1

ER -