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Autosomal recessive variants c.953A>C and c.97-1G>C in NSUN2 causing intellectual disability: a molecular dynamics simulation study of loss-of-function mechanisms

Document Type

Article

Author

Muhammad, N.; Hussain, S.I.; Khan, S.A.; Jan, S.; Khan, N.; Rehman, Z.U.; Muhammad, N.; Khan, S.; Rehman, Z.U.; Muzammal, M.; Khan, M.A.; Abbasi, S.W.; Kakar, N.; Mirza, M.U.; Wasif, N.

Source

In: Frontiers in Neurology. (Frontiers in Neurology, 2023, 14)

Subject

Language

English

ISSN

16642295

Online Access

Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

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