Mutations in the MGAT2 gene controlling complex N-glycan synthesis cause carbohydrate-deficient glycoprotein syndrome type II, an autosomal recessive disease with defective brain development (Q24675799)
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(P31) (Q13442814)
(P304) 810-817
(P407) (Q1860)
(P433) 4
(P478) 59
(P577) Tuesday, October 1, 1996
(P921) (Q1073)
(Q21119445)
(Q14633895)
(Q10267817)
(P1433) (Q4744249)
(P1476) "Mutations in the MGAT2 gene controlling complex N-glycan synthesis cause carbohydrate-deficient glycoprotein syndrome type II, an autosomal recessive disease with defective brain development" (language: en)
(P2093) Tan J
Dunn J
Jaeken J
Schachter H
(P2860) (Q24313186)
(Q24321959)
(Q22066207)
(Q25938983)
(Q28272713)
(Q28588255)
(Q34348805)
(Q40803578)
(Q40769531)
(Q37631574)
(Q34156944)
(Q33624870)
(Q40380586)
(Q36349566)
(Q39735775)
(Q34510875)
(Q37586822)
(Q41256451)
(Q48334324)
(Q44489060)
(Q67973815)
(Q70601195)
(Q72290217)
(Q72316972)
(Q72476085)
(Q59325217)
(Q71865336)
(Q70869007)
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