Mitochondrial diabetes plus phenotypes due to the m.3243A > G variant require correlation with heteroplasmy rates
Author:
Affiliation:
1. Neurology Department Neurology & Neurophysiology Center Vienna Austria
Publisher
Wiley
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.8862
Reference4 articles.
1. The clinical and genetic characteristics of maternally inherited diabetes and deafness (MIDD) with mitochondrial m.3243A > G mutation: A 10‐year follow‐up observation study and literature review
2. Maternally Inherited Diabetes and Deafness (MIDD) – Atypical Clinical Diabetes Features Leading to the Diagnosis
3. Bilateral deafness, diabetes, and different types of cardiomyopathy in family members with m.3243A > g mutation: a case report
4. The Tip of the Iceberg in Maternally Inherited Diabetes and Deafness
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