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Coexistence of mutations in keratin 10 (KRT10) and the mitochondrial genome in a patient with ichthyosis with confetti and Leber's hereditary optic neuropathy

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Description scientific article published on 25 September 2017
Author/s

author: Pawel Kowalski  Cezary Kowalewski  Joanna Kosińska  Agnieszka Kalińska-Bienias  Ewa Pronicka  Urszula Lechowicz  Rafał Płoski  Agnieszka Pollak 

Publication date September 25, 2017
Language English
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