Maternally Inherited Diabetes and Deafness (MIDD)
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-319-66816-1_1838-1
Reference39 articles.
1. Aggarwal P, Gill-Randall R, Wheatley T et al (2001) Identification of mtDNA mutation in a pedigree with gestational diabetes, deafness, Wolff-Parkinson-white syndrome and placenta accreta. Hum Hered 51:114–116. https://doi.org/10.1159/000022950
2. Altmann J, Büchner B, Nadaj-Pakleza A et al (2016) Expanded phenotypic spectrum of the m.8344A > G “MERRF” mutation: data from the German mitoNET registry. J Neurol 263:961–972. https://doi.org/10.1007/s00415-016-8086-3
3. Berkowitz K, Monteagudo A, Marks F et al (1990) Mitochondrial myopathy and preeclampsia associated with pregnancy. Am J Obstet Gynecol 162:146–147. https://doi.org/10.1016/0002-9378(90)90837-W
4. Blackwood JK, Whittaker RG, Blakely EL et al (2010) The investigation and diagnosis of pathogenic mitochondrial DNA mutations in human urothelial cells. Biochem Biophys Res Commun 393:740–745. https://doi.org/10.1016/j.bbrc.2010.02.072
5. Blakely EL, Alston CL, Lecky B et al (2014) Distal weakness with respiratory insufficiency caused by the m.8344A > G “MERRF” mutation. Neuromuscul Disord 24:533–536. https://doi.org/10.1016/j.nmd.2014.03.011
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