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Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder.
Oláhová M, Yoon WH, Thompson K, Jangam S, Fernandez L, Davidson JM, Kyle JE, Grove ME, Fisk DG, Kohler JN, Holmes M, Dries AM, Huang Y, Zhao C, Contrepois K, Zappala Z, Frésard L, Waggott D, Zink EM, Kim YM, Heyman HM, Stratton KG, Webb-Robertson BM; Undiagnosed Diseases Network, Snyder M, Merker JD, Montgomery SB, Fisher PG, Feichtinger RG, Mayr JA, Hall J, Barbosa IA, Simpson MA, Deshpande C, Waters KM, Koeller DM, Metz TO, Morris AA, Schelley S, Cowan T, Friederich MW, McFarland R, Van Hove JLK, Enns GM, Yamamoto S, Ashley EA, Wangler MF, Taylor RW, Bellen HJ, Bernstein JA, Wheeler MT. Oláhová M, et al. Among authors: morris aa. Am J Hum Genet. 2018 Mar 1;102(3):494-504. doi: 10.1016/j.ajhg.2018.01.020. Epub 2018 Feb 22. Am J Hum Genet. 2018. PMID: 29478781 Free PMC article.
Glutaric aciduria and suspected child abuse.
Morris AA, Hoffmann GF, Naughten ER, Monavari AA, Collins JE, Leonard JV. Morris AA, et al. Arch Dis Child. 1999 May;80(5):404-5. doi: 10.1136/adc.80.5.404. Arch Dis Child. 1999. PMID: 10208941 Free PMC article. No abstract available.
Metabolic disorders in children.
Morris AA, Turnbull DM. Morris AA, et al. Curr Opin Neurol. 1994 Dec;7(6):535-41. doi: 10.1097/00019052-199412000-00011. Curr Opin Neurol. 1994. PMID: 7866586 Review.
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