The first concurrent detection of mitochondrial DNA m.3243A>G mutation, deletion, and depletion in a family with mitochondrial diabetes

BACKGROUND: Mitochondrial diabetes (MD) is a rare monogenic form of diabetes and divided into type l and type 2. It is characterized by a strong familial clustering of diabetes with the presence of maternal transmission in conjunction with bilateral hearing impairment in most of the carriers. The mo...

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Detalles Bibliográficos
Autores principales: Tabebi, Mouna, Safi, Wajdi, Felhi, Rahma, Alila Fersi, Olfa, Keskes, Leila, Abid, Mohamed, Mnif, Mouna, Fakhfakh, Faiza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336730/
https://www.ncbi.nlm.nih.gov/pubmed/32394641
http://dx.doi.org/10.1002/mgg3.1292

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336730/
https://www.ncbi.nlm.nih.gov/pubmed/32394641
http://dx.doi.org/10.1002/mgg3.1292

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