Results 201 to 210 of about 6,089,967 (287)

Bi-allelic mutations in FASTKD5 are associated with cytochrome c oxidase deficiency and early- to late-onset Leigh syndrome. [PDF]

open access: yesAm J Hum Genet
Antonicka H   +17 more
europepmc   +1 more source

Anesthetic management in pediatric patient for percutaneous endoscopic gastrostomy with mitochondrial myopathy: Leigh syndrome

open access: green, 2018
Ebru Tarıkçı Kılıç   +4 more
openalex   +1 more source

Phenotypic assessment of Cox10 variants and their implications for Leigh Syndrome. [PDF]

open access: yesBMC Res Notes
Voges TS   +6 more
europepmc   +1 more source

SLC 25A46 is required for mitochondrial lipid homeostasis and cristae maintenance and is responsible for Leigh syndrome

open access: gold, 2016
Alexandre Janer   +12 more
openalex   +1 more source

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