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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

Report for Pena SDJ

General

References (1)

1. 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