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Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome

Document Type

Article

Author

Niceta, M.; Digilio, M.C.; Pizzi, S.; Dentici, M.L.; Dallapiccola, B.; Tartaglia, M.; Margiotti, K.; Guida, V.; Ferraris, A.; Consoli, F.; Torrente, I.; De Luca, A.; Bruselles, A.; Memo, L.; Laforgia, N.; Ruiz-Perez, V.L.; Marino, B.

Source

In: Clinical Genetics. (Clinical Genetics, March 2018, 93(3):632-639)

Subject

Language

English

ISSN

13990004
00099163

Online Access

Full Text (Wiley Journals) Full Text (Wiley-DB) Web of Science JCR 저널정보 Scopus Find it@PNU

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