共 116 条
[1]
Ng YS(2022)Endocrine manifestations and new developments in mitochondrial disease Endocr Rev 46 214-220
[2]
Lim AZ(2008)Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation Diabet Med 37 512-519
[3]
Panagiotou G(2013)A maternally inherited diabetes and deafness patient with the 12S rRNA m.1555A>G and the ND1 m.3308T>C mutations associated with multiple mitochondrial deletions Biochem Biophys Res Commun 28 1039-1057
[4]
Murphy R(2018)Mitochondrial disease: an uncommon but important cause of diabetes mellitus Endocrinol Diabetes Metab Case Rep 33 676-682
[5]
Turnbull DM(2013)The UK MRC mitochondrial disease patient cohort study: clinical phenotypes associated with the m.3243A>G mutation - implications for diagnosis and management J Neurol Neurosurg Psychiatry 45 478-487
[6]
Walker M(2012)Mitochondrial diabetes in children: seek and you will find it PLoS ONE undefined undefined-undefined
[7]
Hattersley AT(2014)Maternally inherited diabetes and deafness (MIDD): diagnosis and management J Diabetes Complicat undefined undefined-undefined
[8]
Mezghani N(2018)mt DNA heteroplasmy level and copy number indicate disease burden in m3243A>G mitochondrial disease EMBO Mol Med undefined undefined-undefined
[9]
Mnif M(2009)The clinical variability of maternally inherited diabetes and deafness is associated with the degree of heteroplasmy in blood leukocytes J Clin Endocrinol Metab undefined undefined-undefined
[10]
Mkaouar-Rebai E(1995)Mutation in the mitochondrial tRNAleu at position 3243 and spontaneous abortions in Japanese women attending a clinic for diabetic pregnancies Diabetologia undefined undefined-undefined