Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 2 (of 2 Records) |
Query Trace: Cytochrome C Oxidase Deficiency[original query] |
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Studies of COX16, COX19, and PET191 in human cytochrome-c oxidase deficiency. Archives of neurology 2004 Dec 61 (12): 1935-7. Tay Stacey K H, Nesti Claudia, Mancuso Michelangelo, Schon Eric A, Shanske Sara, Bonilla Eduardo, Davidson Mercy M, Dimauro Salvato |
High prevalence of SURF1 c.845_846delCT mutation in Polish Leigh patients. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2009 Mar 13 (2): 146-53. Piekutowska-Abramczuk Dorota, Popowska Ewa, Pronicki Maciej, Karczmarewicz Elzbieta, Tylek-Lemanska Dorota, Sykut-Cegielska Jolanta, Szymanska-Dembinska Tamara, Bielecka Liliana, Krajewska-Walasek Malgorzata, Pronicka E |
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