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C2CD3 gene
Known as:
C2CD3
, DKFZP586P0123
, C2 CALCIUM-DEPENDENT DOMAIN-CONTAINING PROTEIN 3
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National Institutes of Health
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2015
2015
Genotype-Phenotype correlations in Joubert Syndrome in the Era of Next Generation Sequencing
R. Bachmann-Gagescu
,
J. Dempsey
,
+6 authors
D. Doherty
Cilia
2015
Corpus ID: 40360486
Results Core JS diagnostic features (hypotonia, ataxia, cognitive dysfunction, oculo-motor apraxia) were present in >80% of…
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