Gene: NDRG4 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 65009
Gene Symbol: NDRG4
NDRG4 		0.010 GeneticVariation disease BEFREE We thus propose that this homozygous variant in NDRG4 may be the causative variant of the autosomal recessive form of IM in the studied family and that it should be investigated in other cases of autosomal recessive infantile myofibromatosis. 25241110 2015