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National Institutes of Health
Semantic Scholar uses AI to extract papers important to this topic.
CODAS syndrome is associated with mutations of LONP1, encoding mitochondrial AAA+ Lon protease.
R. N. Jinks
American journal of human genetics
Corpus ID: 205330910
CODAS syndrome is a multi-system developmental disorder characterized by cerebral, ocular, dental, auricular, and skeletal…
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