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Monoallelic Mutations in CC2D1A Suggest a Novel Role in Human Heterotaxy and Ciliary Dysfunction

Document Type

Article

Author

Ma, A.C.H.; Hasan, K.M.M.; Mak, C.C.Y.; Yeung, K.S.; Pei, S.L.C.; Ying, D.; Yu, M.H.C.; Chow, P.C.; Cheung, Y.F.; Chung, B.H.Y.; Chen, X.

Source

In: Circulation: Genomic and Precision Medicine. (Circulation: Genomic and Precision Medicine, 1 December 2020, 13(6):E003000)

Subject

Language

English

ISSN

25748300

Online Access

Full Text (LWW Journals - Ovid) Full Text (LWW total - Ovid) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

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