Condition: Memory impairment


rs1556424691 in CYTB;ND6;TRNT gene and Memory impairment PMID 22638997 2012 New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset.

PMID 30236074 2018 Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.

PMID 29760464 2018 CO2-sensitive tRNA modification associated with human mitochondrial disease.

PMID 8511015 1993 Mitochondrial disorder associated with newborn cardiopulmonary arrest.

rs2732260 in FUT10 gene and Memory impairment PMID 29724592 2018 Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.

rs1977412 in LOC105373166 gene and Memory impairment PMID 30514930 2018 Genetic data and cognitively defined late-onset Alzheimer's disease subgroups.