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Germline de novo variant F747S extends the phenotypic spectrum of CACNA1D Ca2+ channelopathies

Document Type

Article

Author

Török, F.; Filippini, L.; Zanetti, L.; Drexel, R.S.; Striessnig, J.; Ortner, N.J.; Tezcan, K.; Fernández-Quintero, M.L.; Liedl, K.R.

Source

In: Human Molecular Genetics. (Human Molecular Genetics, 1 March 2023, 32(5):847-859)

Subject

Language

English

ISSN

14602083
09646906

Online Access

Full Text (Oxford University Press) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

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