| 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 |
| Gene_locus related to this paper: human-NDRG4 |
Linhares ND, Freire MCM, Cardenas R, Pena HB, Bahia M, Pena SDJ (2018)
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
Eur Journal of Medical Genetics
61 :106
Linhares ND, Freire MCM, Cardenas R, Pena HB, Bahia M, Pena SDJ (2018)
Eur Journal of Medical Genetics
61 :106