Mutations in the Fukutin-Related Protein Gene (FKRP) Cause a Form of Congenital Muscular Dystrophy with Secondary Laminin α2 Deficiency and Abnormal Glycosylation of α-Dystroglycan

Overview of attention for article published in American Journal of Human Genetics, October 2001

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In the top 25% of all research outputs scored by Altmetric
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