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Loss of function mutations in the gene encoding Omi/HtrA2... | ResearchHub
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Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease
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Authors
Karsten Strauss
14 more
Karsten Strauss
•
L. Martins
12 more
•
Rejko Krüger
Published
June 16, 2005
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Journal
Human Molecular Genetics
Topics
Biology
Internal Medicine
Medicine
Neurology
Cellular And Molecular Neuroscience
Show all topics
DOI
10.1093/hmg/ddi215
