Freire MCM

References (1)

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