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Year | Number of Results |
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2008 | 1 |
2009 | 2 |
2024 | 0 |
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Molecular and clinical genetics of mitochondrial diseases due to POLG mutations.
Hum Mutat. 2008 Sep;29(9):E150-72. doi: 10.1002/humu.20824.
Hum Mutat. 2008.
PMID: 18546365
Free PMC article.
Infantile cardiomyopathy caused by a mutation in the overlapping region of mitochondrial ATPase 6 and 8 genes.
Ware SM, El-Hassan N, Kahler SG, Zhang Q, Ma YW, Miller E, Wong B, Spicer RL, Craigen WJ, Kozel BA, Grange DK, Wong LJ.
Ware SM, et al.
J Med Genet. 2009 May;46(5):308-14. doi: 10.1136/jmg.2008.063149. Epub 2009 Feb 2.
J Med Genet. 2009.
PMID: 19188198
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Application of dual-genome oligonucleotide array-based comparative genomic hybridization to the molecular diagnosis of mitochondrial DNA deletion and depletion syndromes.
Chinault AC, Shaw CA, Brundage EK, Tang LY, Wong LJ.
Chinault AC, et al.
Genet Med. 2009 Jul;11(7):518-26. doi: 10.1097/GIM.0b013e3181abd83c.
Genet Med. 2009.
PMID: 19546809
Free article.
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