Author:
White Sarah L.,Collins Veronica R.,Wolfe Rory,Cleary Maureen A.,Shanske Sara,DiMauro Salvatore,Dahl Hans-Henrik M.,Thorburn David R.
Subject
Genetics (clinical),Genetics
Reference44 articles.
1. Prenatal diagnosis of T8993G mitochondrial DNA point mutation in amniocytes by heteroplasmy detection;Bartley;Am J Hum Genet,1996
2. Skewed segregation of the mtDNA nt 8993 (T→G) mutation in human oocytes;Blok;Am J Hum Genet,1997
3. Distribution and threshold expression of the tRNALys mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF);Boulet;Am J Hum Genet,1992
4. Molecular pathology of MELAS and MERRF: the relationship between mutation load and clinical phenotypes;Chinnery;Brain,1997
5. Maternally inherited Leigh syndrome;Ciafaloni;J Pediatr,1993
Cited by
173 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献