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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 |