Mutations in STT3A and STT3B cause two congenital disorders of glycosylation

Shiteshu Shrimal(University of Massachusetts Chan Medical School), Hudson H. Freeze(Discovery Institute), Marie‐Estelle Losfeld(Sanford Burnham Prebys Medical Discovery Institute), Reid Gilmore(University of Massachusetts Chan Medical School), B. G. Ng(Sanford Burnham Prebys Medical Discovery Institute)
Human Molecular Genetics
July 10, 2013
Cited by 86


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