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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 1
2005 1
2006 2
2008 1
2011 1
2013 1
2017 1
2018 1
2021 1
2024 0

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PubMed for id: 767302

9 results

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Page 1
Congenital muscular dystrophy type 1D (MDC1D) due to a large intragenic insertion/deletion, involving intron 10 of the LARGE gene.
Clarke NF, Maugenre S, Vandebrouck A, Urtizberea JA, Willer T, Peat RA, Gray F, Bouchet C, Manya H, Vuillaumier-Barrot S, Endo T, Chouery E, Campbell KP, Mégarbané A, Guicheney P. Clarke NF, et al. Eur J Hum Genet. 2011 Apr;19(4):452-7. doi: 10.1038/ejhg.2010.212. Epub 2011 Jan 19. Eur J Hum Genet. 2011. PMID: 21248746 Free PMC article.
Glycosylation defects in inherited muscle disease.
Hewitt JE, Grewal PK. Hewitt JE, et al. Cell Mol Life Sci. 2003 Feb;60(2):251-8. doi: 10.1007/s000180300020. Cell Mol Life Sci. 2003. PMID: 12678490 Free PMC article. Review.