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3 matching publication(s)
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase.
PMID 16964263 · Nature genetics · 2006
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No data access
Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome.
PMID 17033964 · · 2006
L1
75/100
AlphaPIX and betaPIX and their role in focal adhesion formation.
PMID 16337026 · · 2006
L1
No computation