Novel mitochondrial DNA mutations associated with myopathy, cardiomyopathy, renal failure, and deafness.
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| Title: | Novel mitochondrial DNA mutations associated with myopathy, cardiomyopathy, renal failure, and deafness. |
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| Authors: | Feigenbaum A; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada., Bai RK, Doherty ES, Kwon H, Tan D, Sloane A, Cutz E, Robinson BH, Wong LJ |
| Source: | American journal of medical genetics. Part A [Am J Med Genet A] 2006 Oct 15; Vol. 140 (20), pp. 2216-22. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print Cited Medium: Print ISSN: 1552-4825 (Print) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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