Report for Linhares ND

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References (2)

Title : Exome sequencing identifies a novel homozygous variant in NDRG4 in a family with infantile myofibromatosis (Linhares et al., 2014) turns out to be EBV+ leiomyomatosis caused by CARMIL2 mutations -
Author(s) : Linhares ND , Freire MCM , Cardenas R , Pena HB , Bahia M , Pena SDJ
Ref : Eur Journal of Medical Genetics , 61 :106 , 2018
PubMedID: 28223207
Gene_locus related to this paper: human-NDRG4

Title : Exome sequencing identifies a novel homozygous variant in NDRG4 in a family with infantile myofibromatosis - Linhares_2014_Eur.J.Med.Genet_57_643
Author(s) : Linhares ND , Freire MC , Cardenas RG , Pena HB , Bahia M , Pena SD
Ref : Eur Journal of Medical Genetics , 57 :643 , 2014
Abstract : Linhares_2014_Eur.J.Med.Genet_57_643
ESTHER : Linhares_2014_Eur.J.Med.Genet_57_643
PubMedSearch : Linhares_2014_Eur.J.Med.Genet_57_643
PubMedID: 25241110
Gene_locus related to this paper: human-NDRG4