검색결과 : 3건
| No. | Article |
|---|---|
| 1 |
A novel splicing mutation in the ABCA1 gene, causing Tangier disease and familial HDL deficiency in a large family Maranghi M, Truglio G, Gallo A, Grieco E, Verrienti A, Montali A, Gallo P, Alesini F, Arca M, Lucarelli M Biochemical and Biophysical Research Communications, 508(2), 487, 2019 |
| 2 |
Cytochrome C oxydase deficiency: SURF1 gene investigation in patients with Leigh syndrome Maalej M, Kammoun T, Alila-Fersi O, Kharrat M, Ammar M, Felhi R, Mkaouar-Rebai E, Keskes L, Hachicha M, Fakhfakh F Biochemical and Biophysical Research Communications, 497(4), 1043, 2018 |
| 3 |
Carrier protein import into mitochondria mediated by the intermembrane proteins Tim10/Mrs11 and Tim12/Mrs5 Sirrenberg C, Endres M, Folsch H, Stuart RA, Neupert W, Brunner M Nature, 391(6670), 912, 1998 |