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A homozygous founder variant in PDE2A causes paroxysmal dyskinesia with intellectual disability

Document Type

Article

Author

Yousaf, H.; Jameel, M.; Saadi, S.M.; Tariq, M.; Baig, S.M.; Rehmat, S.; Ibrahim, R.; Hashmi, S.N.; Fatima, A.; Makhdoom, E.U.H.; Iwaszkiewicz, J.; Toft, M.; Iqbal, Z.

Source

In: Clinical Genetics. (Clinical Genetics, September 2023, 104(3):324-333)

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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