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Mutations in DDX58, which Encodes RIG-I, Cause Atypical S... | ResearchHub
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Mutations in DDX58, which Encodes RIG-I, Cause Atypical Singleton-Merten Syndrome
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Authors
Mi‐Ae Jang
25 more
Mi‐Ae Jang
•
Eun Kim
23 more
•
Chang‐Seok Ki
Published
January 22, 2015
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Journal
The American Journal of Human Genetics
Topics
Biology
Neuroscience
Medicine
Immunology
Internal Medicine
Show all topics
DOI
10.1016/j.ajhg.2014.11.019
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publisher-specific-oa
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Journal
The American Journal of Human Genetics
Topics
Biology
Neuroscience
Medicine
Immunology
Internal Medicine
Show all topics
DOI
10.1016/j.ajhg.2014.11.019
License
publisher-specific-oa
