Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Hypoglycemia and ACADVL[original query] |
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Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States. Molecular genetics and metabolism 2015 Sep . Miller Marcus J, Burrage Lindsay C, Gibson James B, Strenk Meghan E, Lose Edward J, Bick David P, Elsea Sarah H, Sutton V Reid, Sun Qin, Graham Brett H, Craigen William J, Zhang Victor Wei, Wong Lee-Jun |
Molecular and clinical characteristics of very-long-chain acyl-CoA dehydrogenase deficiency: A single-center experience in Saudi Arabia. Saudi medical journal 2020 6 41 (6): 590-596. Alhashem Amal, Mohamed Sarar, Abdelraheem Manal, AlGufaydi Bushra, Al-Aqeel Ai |
Outcomes of mitochondrial long chain fatty acid oxidation and carnitine defects from a single center metabolic genetics clinic. Orphanet journal of rare diseases 2022 9 17 (1): 360. Ambrose Anastasia, Sheehan Melissa, Bahl Shalini, Athey Taryn, Ghai-Jain Shailly, Chan Alicia, Mercimek-Andrews Saad |
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- Page last updated:Apr 22, 2024
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