| 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 : |
| PubMedSearch : Linhares_2014_Eur.J.Med.Genet_57_643 |
| PubMedID: 25241110 |
| Gene_locus related to this paper: human-NDRG4 |