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Year | Number of Results |
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2007 | 2 |
2008 | 1 |
2024 | 0 |
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New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutation.
Neurology. 2007 Sep 18;69(12):1254-60. doi: 10.1212/01.wnl.0000268489.60809.c4. Epub 2007 Jul 18.
Neurology. 2007.
PMID: 17634419
Free article.
Protein O-mannosyltransferase activities in lymphoblasts from patients with alpha-dystroglycanopathies.
Manya H, Bouchet C, Yanagisawa A, Vuillaumier-Barrot S, Quijano-Roy S, Suzuki Y, Maugenre S, Richard P, Inazu T, Merlini L, Romero NB, Leturcq F, Bezier I, Topaloglu H, Estournet B, Seta N, Endo T, Guicheney P.
Manya H, et al.
Neuromuscul Disord. 2008 Jan;18(1):45-51. doi: 10.1016/j.nmd.2007.08.002. Epub 2007 Sep 14.
Neuromuscul Disord. 2008.
PMID: 17869517
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