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Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylation

Document Type

Article

Author

Ng, B.G.; Eroshkin, A.; Losfeld, M.E.; Freeze, H.H.; Buckingham, K.J.; Chong, J.X.; Bamshad, M.J.; Raymond, K.; Kircher, M.; Turner, E.H.; Smith, J.D.; Nickerson, D.A.; Shendure, J.; He, M.; Szybowska, M.; Kozenko, M.; Li, C.; Patterson, M.C.; Gilbert, R.D.

Source

In: American Journal of Human Genetics. (American Journal of Human Genetics, 4 April 2013, 92(4):632-636)

Subject

Language

English

ISSN

00029297
15376605

Online Access

Full Text (ScienceDirect 종량제) Full Text (ScienceDirect O/A) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

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