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GLYCOSYLATION DISORDER SYNDROME TYPE 1b: DIAGNOSTICS AND TREATMENT

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The article highlights the medical case of a rare hereditary disease - glycosylation disorder syndrome type 1b, unique for our country. This syndrome is referred to the heterogeneous group of the congenital diseases characterized by the disorder of glycoprotein synthesis as a result of the defects N...

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Main Authors: Yu.S. Akoev (Author), A.V. Migali (Author), N.V. Zhurkova (Author), O.B. Kondakova (Author), E.A. Roslavtseva (Author), A.R. Pinaeva (Author), V.A. Skvortsova (Author), I.I. Migali (Author)
Format: Book
Published: Union of pediatricians of Russia, 2008-09-01T00:00:00Z.
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