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1987 | 1 |
1993 | 1 |
2024 | 0 |
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A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome.
Ann Neurol. 1993 Sep;34(3):410-2. doi: 10.1002/ana.410340319.
Ann Neurol. 1993.
PMID: 8395787
Familial Leigh's syndrome: association with a defect in oxidative metabolism probably restricted to brain.
van Erven PM, Gabreëls FJ, Ruitenbeek W, Renier WO, Lamers KJ, Sloof JL.
van Erven PM, et al.
J Neurol. 1987 May;234(4):215-9. doi: 10.1007/BF00618253.
J Neurol. 1987.
PMID: 3612192
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