Mitochondrial disorders
Gene: NDUFA10
only one patient reported in literature to dateCreated: 3 Feb 2016, 4:50 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Victorian Clinical Genetics Services was added to NDUFA10. Panel: Mitochondrial disorders
Model of inheritance for gene NDUFA10 was changed to BIALLELIC, autosomal or pseudoautosomal
NDUFA10 was added to All recognised syndromes and those with suggestive featurespanel. Sources: Expert,Expert list,Radboud University Medical Center, Nijmegen,Emory Genetics Laboratory,Illumina TruGenome Clinical Sequencing Services
Model of inheritance for gene NDUFA10 was changed to BIALLELIC, autosomal or pseudoautosomal
NDUFA10 was added to All recognised syndromes and those with suggestive featurespanel. Sources: Expert,Expert list,Radboud University Medical Center, Nijmegen,Emory Genetics Laboratory,Illumina TruGenome Clinical Sequencing Services
Model of inheritance for gene NDUFA10 was changed to BIALLELIC, autosomal or pseudoautosomal
NDUFA10 was added to All recognised syndromes and those with suggestive featurespanel. Sources: Expert,Expert list,Radboud University Medical Center, Nijmegen,Emory Genetics Laboratory,Illumina TruGenome Clinical Sequencing Services
Model of inheritance for gene NDUFA10 was changed to BIALLELIC, autosomal or pseudoautosomal
NDUFA10 was added to All recognised syndromes and those with suggestive featurespanel. Sources: Expert,Expert list,Radboud University Medical Center, Nijmegen,Emory Genetics Laboratory,Illumina TruGenome Clinical Sequencing Services
NDUFA10 was added to All recognised syndromes and those with suggestive featurespanel. Sources: Expert,Expert list,Radboud University Medical Center, Nijmegen,Emory Genetics Laboratory,Illumina TruGenome Clinical Sequencing Services