검색결과 : 3건
| No. | Article |
|---|---|
| 1 |
A novel mutation MT-COIII m.9267G > C and MT-COI m.5913G > A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with sever nephropathy Tabebi M, Mkaouar-Rebai E, Mnif M, Kallabi F, Ben Mahmoud A, Ben Saad W, Charfi N, Keskes-Ammar L, Kamoun H, Abid M, Fakhfakh F Biochemical and Biophysical Research Communications, 459(3), 353, 2015 |
| 2 |
Accumulation of pathogenic Delta mtDNA induced deafness but not diabetic phenotypes in mito-mice Nakada K, Sato A, Sone H, Kasahara A, Ikeda K, Kagawa Y, Yonekawa H, Hayashi J Biochemical and Biophysical Research Communications, 323(1), 175, 2004 |
| 3 |
Mitochondrial DNA variations in patients with maternally inherited diabetes and deafness syndrome Perucca-Lostanlen D, Narbonne H, Hernandez JB, Staccini P, Saunieres A, Paquis-Flucklinger V, Vialettes B, Desnuelle C Biochemical and Biophysical Research Communications, 277(3), 771, 2000 |