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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2001 | 1 |
2003 | 1 |
2004 | 1 |
2024 | 0 |
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Page 1
POMGnT1 mutation and phenotypic spectrum in muscle-eye-brain disease.
J Med Genet. 2004 Oct;41(10):e115. doi: 10.1136/jmg.2004.020701.
J Med Genet. 2004.
PMID: 15466003
Free PMC article.
No abstract available.
Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease.
Taniguchi K, Kobayashi K, Saito K, Yamanouchi H, Ohnuma A, Hayashi YK, Manya H, Jin DK, Lee M, Parano E, Falsaperla R, Pavone P, Van Coster R, Talim B, Steinbrecher A, Straub V, Nishino I, Topaloglu H, Voit T, Endo T, Toda T.
Taniguchi K, et al.
Hum Mol Genet. 2003 Mar 1;12(5):527-34. doi: 10.1093/hmg/ddg043.
Hum Mol Genet. 2003.
PMID: 12588800
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Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1.
Yoshida A, Kobayashi K, Manya H, Taniguchi K, Kano H, Mizuno M, Inazu T, Mitsuhashi H, Takahashi S, Takeuchi M, Herrmann R, Straub V, Talim B, Voit T, Topaloglu H, Toda T, Endo T.
Yoshida A, et al.
Dev Cell. 2001 Nov;1(5):717-24. doi: 10.1016/s1534-5807(01)00070-3.
Dev Cell. 2001.
PMID: 11709191
Free article.
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