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Year | Number of Results |
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2003 | 1 |
2019 | 2 |
2020 | 1 |
2024 | 0 |
PubMed (cited) for id: 616715
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TMX2 Is a Crucial Regulator of Cellular Redox State, and Its Dysfunction Causes Severe Brain Developmental Abnormalities.
Am J Hum Genet. 2019 Dec 5;105(6):1126-1147. doi: 10.1016/j.ajhg.2019.10.009. Epub 2019 Nov 14.
Am J Hum Genet. 2019.
PMID: 31735293
Free PMC article.
Recurrent homozygous damaging mutation in TMX2, encoding a protein disulfide isomerase, in four families with microlissencephaly.
Ghosh SG, Wang L, Breuss MW, Green JD, Stanley V, Yang X, Ross D, Traynor BJ, Alhashem AM, Azam M, Selim L, Bastaki L, Elbastawisy HI, Temtamy S, Zaki M, Gleeson JG.
Ghosh SG, et al.
J Med Genet. 2020 Apr;57(4):274-282. doi: 10.1136/jmedgenet-2019-106409. Epub 2019 Oct 5.
J Med Genet. 2020.
PMID: 31586943
Free PMC article.
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Cloning and identification of a novel cDNA coding thioredoxin-related transmembrane protein 2.
Meng X, Zhang C, Chen J, Peng S, Cao Y, Ying K, Xie Y, Mao Y.
Meng X, et al.
Biochem Genet. 2003 Apr;41(3-4):99-106. doi: 10.1023/a:1022073917044.
Biochem Genet. 2003.
PMID: 12670024
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