RMND1 deficiency associated with neonatal lactic acidosis, infantile onset renal failure, deafness, and multiorgan involvement.
European journal of human genetics : EJHG | 2015-10-01 | PMID 25604853
Janer Alexandre, van Karnebeek Clara Dm, Sasarman Florin and 10 more
Genes: RMND1
