Molecular interaction between fukutin and POMGnT1 in the glycosylation pathway of α-dystroglycan

H Xiong, K Kobayashi, M Tachikawa, H Manya… - Biochemical and …, 2006 - Elsevier
The recent identification of mutations in genes encoding demonstrated or putative
glycosyltransferases has revealed a novel mechanism for congenital muscular dystrophy …
被引用次数：92 相关文章

Molecular interaction between fukutin and POMGnT1 in the glycosylation pathway of α-dystroglycan

H Xiong, K Kobayashi, M Tachikawa, H Manya… - Biochemical and …, 2006 - infona.pl
The recent identification of mutations in genes encoding demonstrated or putative
glycosyltransferases has revealed a novel mechanism for congenital muscular dystrophy …

Molecular interaction between fukutin and POMGnT1 in the glycosylation pathway of alpha-dystroglycan

H Xiong, K Kobayashi, M Tachikawa… - Biochemical and …, 2006 - pubmed.ncbi.nlm.nih.gov
The recent identification of mutations in genes encoding demonstrated or putative
glycosyltransferases has revealed a novel mechanism for congenital muscular dystrophy …
[PDF] academia.edu

[PDF][PDF] Molecular interaction between fukutin and POMGnT1 in the glycosylation pathway of a-dystroglycan

H Xiong, K Kobayashi, M Tachikawa… - Biochemical and …, 2006 - academia.edu
The recent identification of mutations in genes encoding demonstrated or putative
glycosyltransferases has revealed a novel mechanism for congenital muscular dystrophy …

[引用][C] Molecular interaction between fukutin and POMGnT1 in the glycosylation pathway of α-dystroglycan

H Xiong, K Kobayashi, M Tachikawa, H Manya… - Biochemical and …, 2006 - cir.nii.ac.jp
Molecular interaction between fukutin and POMGnT1 in the glycosylation pathway of α-dystroglycan
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Molecular interaction between fukutin and POMGnT1 in the glycosylation pathway of alpha-dystroglycan.

H Xiong, K Kobayashi, M Tachikawa… - Biochemical and …, 2006 - europepmc.org
The recent identification of mutations in genes encoding demonstrated or putative
glycosyltransferases has revealed a novel mechanism for congenital muscular dystrophy …