Clustering of Alpers disease mutations and catalytic defects in biochemical variants reveal new features of molecular mechanism of the human mitochondrial replicase, Pol γ
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Title
Clustering of Alpers disease mutations and catalytic defects in biochemical variants reveal new features of molecular mechanism of the human mitochondrial replicase, Pol γ
Authors
Keywords
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Journal
NUCLEIC ACIDS RESEARCH
Volume 39, Issue 21, Pages 9072-9084
Publisher
Oxford University Press (OUP)
Online
2011-08-09
DOI
10.1093/nar/gkr618
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