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Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease
by
Kösel, S
,
Grasbon-Frodl, E M
,
Mautsch, U
,
Egensperger, R
,
von Eitzen, U
,
Frishman, D
,
Hofmann, S
,
Gerbitz, K D
,
Mehraein, P
,
Graeber, M B
Published in
Neurogenetics
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Neurogenetics
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Amino Acid Sequence
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Amino Acid Substitution
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Clinical Neurology
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Dna Mutational Analysis
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Dna, Mitochondrial - Chemistry
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Gene Frequency
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Genetic Heterogeneity
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Neurosciences & Neurology
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