CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow
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Date
Journal Title
Journal ISSN
Volume Title
dc.identifier.issn
dc.identifier.doi
10.26508/lsa.202402708
dc.identifier.other
WOS:001458798700001
dc.description.volume
dc.description.issue
Publisher
LIFE SCIENCE ALLIANCE LLC
DOI
10.26508/lsa.202402708