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Concomitant partial exon skipping by a unique missense mutation of RPS6KA3 causes Coffin-Lowry syndrome

Document Type

Article

Author

Labonne, J.D.J.; Chung, M.J.; Layman, L.C.; Kim, H.-G.; Jones, J.R.; Anand, P.; Wenzel, W.; Iacoboni, D.

Source

In: Gene. (Gene, 1 January 2016, 575(1):42-47)

Subject

Language

English

ISSN

18790038
03781119

Online Access

Full Text (ScienceDirect 종량제) Full Text (ScienceDirect) Web of Science JCR 저널정보 Scopus Find it@PNU

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