1. 1. Suzuki J, Iwata M, Moriyoshi H, Nishida S, Yasuda T, Ito Y. Familial pernicious chronic intestinal pseudo-obstruction with a mitochondrial DNA A3243G mutation. Intern Med 56: 1089-1093, 2017.
2. 2. Mancuso M, Orsucci D, Angelini C, et al. "Mitochondrial neuropathies": A survey from the large cohort of the Italian Network. Neuromuscul Disord 26: 272-276, 2016.
3. 3. Rankin J, Brown R, Dobyns WB, et al. Pontocerebellar hypoplasia type 6: A British case with PEHO-like features. Am J Med Genet A 152A: 2079-2084, 2010.
4. 4. Mancuso M, Orsucci D, Angelini C, et al. The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender? J Neurol 261: 504-510, 2014.
5. 5. Finsterer J, Frank M. Gastrointestinal manifestations of mitochondrial disorders: a systematic review. Therap Adv Gastroenterol 10: 142-154, 2017.