Coexistence of mutations in keratin 10 (KRT10) and the mitochondrial genome in a patient with ichthyosis with confetti and Leber's hereditary optic neuropathy
published in: American Journal of Medical Genetics
date of publication: 2017-09-25
language: English
main subject: hereditary optic neuropathy, Ichthyosis with confetti
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Article - wd:Q59697352