Liao_2013_Eur.J.Med.Genet_56_484

Reference

Title : Loss-of-function variation in the DPP6 gene is associated with autosomal dominant microcephaly and mental retardation - Liao_2013_Eur.J.Med.Genet_56_484
Author(s) : Liao C , Fu F , Li R , Yang WQ , Liao HY , Yan JR , Li J , Li SY , Yang X , Li DZ
Ref : Eur Journal of Medical Genetics , 56 :484 , 2013
Abstract : Liao_2013_Eur.J.Med.Genet_56_484
ESTHER : Liao_2013_Eur.J.Med.Genet_56_484
PubMedSearch : Liao_2013_Eur.J.Med.Genet_56_484
PubMedID: 23832105
Gene_locus related to this paper: human-DPP6

Related information

Gene_locus related to this paper: human-DPP6

Citations formats

Liao C, Fu F, Li R, Yang WQ, Liao HY, Yan JR, Li J, Li SY, Yang X, Li DZ (2013)
Loss-of-function variation in the DPP6 gene is associated with autosomal dominant microcephaly and mental retardation
Eur Journal of Medical Genetics 56 :484

Liao C, Fu F, Li R, Yang WQ, Liao HY, Yan JR, Li J, Li SY, Yang X, Li DZ (2013)
Eur Journal of Medical Genetics 56 :484