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MADD gene

Discuss publications and research concerning the MADD gene.

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Related literature

First report of neonatal-onset glutaric aciduria type II in the Iranian population caused by a novel deleterious ETFA variant.
MADD
Neurodevelopmental disorder mutations in the exchange factor DENN/MADD disrupt activation of Rab GTPases.
MADD
Targeted multi-layer analysis of PANoptosis-associated genes in the etiology of chronic kidney disease.
MADD
Brain and blood transcriptome-wide association studies identify five novel genes associated with Alzheimer's disease.
MADD
Large-scale exome sequencing identified 18 novel genes for neuroticism in 394,005 UK-based individuals.
MADD
Sensory neuropathy as a manifestation of multiple acyl-coenzyme A dehydrogenase deficiency.
MADD
The male-to-female ratio in late-onset multiple acyl-CoA dehydrogenase deficiency: a systematic review and meta-analysis.
MADD
Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study.
MADD
Coexistence of Multiple Functional Variants and Genes Underlies Genetic Risk Locus 11p11.2 of Alzheimer's Disease.
MADD
Bivariate Genome-Wide Association Study of Depressive Symptoms With Type 2 Diabetes and Quantitative Glycemic Traits.
MADD

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