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Morin, Gilles; Biancalana, Valérie; Echaniz-Laguna, Andoni; Noury, Jean-Baptiste; Lornage, Xavière; Moggio, Maurizio; Ripolone, Michela; Violano, Raffaella; Marcorelles, Pascale; Maréchal, Denis; Renaud, Florence; Maurage, Claude-Alain; Tard, Céline; Cuisset, Jean-Marie; Laporte, Jocelyn (January 2020). "Tubular aggregate myopathy and Stormorken syndrome: Mutation spectrum and genotype/phenotype correlation". Human Mutation. Forty one (1): 17-37. doi:10.1002/humu.23899. Grassi, Mara; Laubscher, Bernard; Pandey, Amit V.; Tschumi, Sibylle; Graber, Franziska; Schaller, André; Janner, Marco; Aeberli, Daniel; Hewer, Ekkehard; Nuoffer, Jean-Marc; Gautschi, Matthias (August 2023). "Expanding the p.(Arg85Trp) Variant-Specific Phenotype of HNF4A: Features of Glycogen Storage Disease, Liver Cirrhosis, Impaired Mitochondrial Function, and Glomerular Changes". Stanik, Juraj; Skopkova, Martina; Brennerova, Katarina; Danis, Daniel; Rosolankova, Monika; Salingova, Anna; Bzduch, Vladimir; Klimes, Iwar; Gasperikova, Daniela (April 2017). "Congenital hyperinsulinism and glycogenosis-like phenotype on account of a novel HNF4A mutation". Diabetes Research and Clinical Practice. NORD (National Organization for Rare Disorders). Løkken, Nicoline; Hansen, Kit K.; Storgaard, Jesper H.; Ørngreen, Mette C.; Quinlivan, Healthy Flow Blood pills Ros; Vissing, John (July 2020). "Titrating a modified ketogenic diet for patients with McArdle disease: A pilot study".

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