All individuals with variants in gene TRMT10C

3 entries on 1 page. Showing entries 1 - 3.
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00064757 - PubMed: Metodiev 2016, Journal: Metodiev 2016 2-generation family, 1 affected, unaffected heterozygous carrier parents M no United Kingdom (Great Britain) white, British 00y05m - - - mitochondrial respiratory chain deficiency see paper; ..., myopathy, hypotonia, sensorineural deafness, liver involvement; elevated serum and CSF lactate levels; COX-deficient, ragged-red fibers; deceased from respiratory failure 2 1 Johan den Dunnen
00064758 - PubMed: Metodiev 2016, Journal: Metodiev 2016 2-generation family, 1 affected, unaffected heterozygous carrier parents F no - Kurdish 00y05m - - - mitochondrial respiratory chain deficiency see paper; ..., hypotonia, deafness; elevated serum, urine, and CSF lactate levels; deceased respiratory failure 1 1 Johan den Dunnen
00395614 RP-3055 PubMed: Perea-Romero 2021 - - - Spain - - - - - retinal disease cataract, glaucoma, rod-cone dystrophy, severe myopia, conductive hearing impairment, intellectual disability, renal atrophy, renal insufficiency 1 1 LOVD
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