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Year | Number of Results |
---|---|
1998 | 1 |
2002 | 2 |
2023 | 0 |
PubMed (OMIM) for id: 1731194
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Complex neurologic syndrome associated with the G1606A mutation of mitochondrial DNA.
Arch Neurol. 2002 Jun;59(6):1013-5. doi: 10.1001/archneur.59.6.1013.
Arch Neurol. 2002.
PMID: 12056939
Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutation.
McFarland R, Clark KM, Morris AA, Taylor RW, Macphail S, Lightowlers RN, Turnbull DM.
McFarland R, et al.
Nat Genet. 2002 Feb;30(2):145-6. doi: 10.1038/ng819. Epub 2002 Jan 22.
Nat Genet. 2002.
PMID: 11799391
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A novel mutation in the mitochondrial tRNA(Val) gene associated with a complex neurological presentation.
Tiranti V, D'Agruma L, Pareyson D, Mora M, Carrara F, Zelante L, Gasparini P, Zeviani M.
Tiranti V, et al.
Ann Neurol. 1998 Jan;43(1):98-101. doi: 10.1002/ana.410430116.
Ann Neurol. 1998.
PMID: 9450773
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