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Year | Number of Results |
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2013 | 1 |
2014 | 1 |
2024 | 0 |
PubMed for id: 698848593
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TRMT10A dysfunction is associated with abnormalities in glucose homeostasis, short stature and microcephaly.
J Med Genet. 2014 Sep;51(9):581-6. doi: 10.1136/jmedgenet-2014-102282. Epub 2014 Jul 22.
J Med Genet. 2014.
PMID: 25053765
tRNA methyltransferase homolog gene TRMT10A mutation in young onset diabetes and primary microcephaly in humans.
Igoillo-Esteve M, Genin A, Lambert N, Désir J, Pirson I, Abdulkarim B, Simonis N, Drielsma A, Marselli L, Marchetti P, Vanderhaeghen P, Eizirik DL, Wuyts W, Julier C, Chakera AJ, Ellard S, Hattersley AT, Abramowicz M, Cnop M.
Igoillo-Esteve M, et al.
PLoS Genet. 2013 Oct;9(10):e1003888. doi: 10.1371/journal.pgen.1003888. Epub 2013 Oct 31.
PLoS Genet. 2013.
PMID: 24204302
Free PMC article.
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