POMT1 mutation results in defective glycosylation and loss of laminin-binding activity in -DG-Reference-Cited by-同舟云学术

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POMT1 mutation results in defective glycosylation and loss of laminin-binding activity in -DG

Published:2004-03-22 Issue:6 Volume:62 Page:1009-1011
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Kim D. -S.,Hayashi Y. K.,Matsumoto H.,Ogawa M.,Noguchi S.,Murakami N.,Sakuta R.,Mochizuki M.,Michele D. E.,Campbell K. P.,Nonaka I.,Nishino I.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 78 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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5. Congenital muscular dystrophy due to POMGNT1 mutation presenting as cardioembolic stroke;Annals of Indian Academy of Neurology;2022

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