A case of Kearns–Sayre syndrome with two novel deletions (9.768 and 7.253 kb) of the mtDNA associated with the common deletion in blood leukocytes, buccal mucosa and hair follicles
| Autor: | Mkaouar-Rebai, Emna, Chamkha, Imen, Kammoun, Thouraya, Chabchoub, Imen, Aloulou, Hajer, Fendri, Nourhene, Hachicha, Mongia, Fakhfakh, Faiza |
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| Zdroj: | In Mitochondrion 2010 10(5):449-455 |
| Databáze: | ScienceDirect |
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