Dystrophin Gene Mutation Location and the Risk of Cognitive Impairment in Duchenne Muscular Dystrophy-Reference-Cited by-同舟云学术

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Dystrophin Gene Mutation Location and the Risk of Cognitive Impairment in Duchenne Muscular Dystrophy

Published:2010-01-20 Issue:1 Volume:5 Page:e8803
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Taylor Peter J.,Betts Grant A.,Maroulis Sarah,Gilissen Christian,Pedersen Robyn L.,Mowat David R.,Johnston Heather M.,Buckley Michael F.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Cited by 148 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

1. Identifying inversions with breakpoints in the Dystrophin gene through long-read sequencing: report of two cases;BMC Medical Genomics;2024-09-09

2. Early motor, cognitive, language, behavioural and social emotional development in infants and young boys with Duchenne Muscular Dystrophy- A systematic review;European Journal of Paediatric Neurology;2024-09

3. Social and emotional alterations in mice lacking the short dystrophin-gene product, Dp71;Behavioral and Brain Functions;2024-08-24

4. Investigating the Involvement of C−X−C Motif Chemokine 5 and P2X7 Purinoceptor in Ectopic Calcification in Mouse Models of Duchenne Muscular Dystrophy;Journal of Cellular Biochemistry;2024-06-25

5. Learning, memory and blood–brain barrier pathology in Duchenne muscular dystrophy mice lacking Dp427, or Dp427 and Dp140;Genes, Brain and Behavior;2024-06

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