Mitochondrial disorders
Gene: NDUFA11
only one report in literature - six patients from three unrelated familiesCreated: 3 Feb 2016, 4:53 p.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Victorian Clinical Genetics Services was added to NDUFA11. Panel: Mitochondrial disorders
Model of inheritance for gene NDUFA11 was changed to BIALLELIC, autosomal or pseudoautosomal
NDUFA11 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 NDUFA11 was changed to BIALLELIC, autosomal or pseudoautosomal
NDUFA11 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 NDUFA11 was changed to BIALLELIC, autosomal or pseudoautosomal
NDUFA11 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 NDUFA11 was changed to BIALLELIC, autosomal or pseudoautosomal
NDUFA11 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
NDUFA11 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