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Year | Number of Results |
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2010 | 1 |
2015 | 2 |
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PubMed (cited) for id: 616737
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Functional Dysregulation of CDC42 Causes Diverse Developmental Phenotypes.
Am J Hum Genet. 2018 Feb 1;102(2):309-320. doi: 10.1016/j.ajhg.2017.12.015. Epub 2018 Jan 25.
Am J Hum Genet. 2018.
PMID: 29394990
Free PMC article.
Further evidence of a mutation in CDC42 as a cause of a recognizable syndromic form of thrombocytopenia.
Takenouchi T, Okamoto N, Ida S, Uehara T, Kosaki K.
Takenouchi T, et al.
Am J Med Genet A. 2016 Apr;170A(4):852-5. doi: 10.1002/ajmg.a.37526. Epub 2015 Dec 28.
Am J Med Genet A. 2016.
PMID: 26708094
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Macrothrombocytopenia and developmental delay with a de novo CDC42 mutation: Yet another locus for thrombocytopenia and developmental delay.
Takenouchi T, Kosaki R, Niizuma T, Hata K, Kosaki K.
Takenouchi T, et al.
Am J Med Genet A. 2015 Nov;167A(11):2822-5. doi: 10.1002/ajmg.a.37275. Epub 2015 Aug 6.
Am J Med Genet A. 2015.
PMID: 26386261
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Multiple alterations of platelet functions dominated by increased secretion in mice lacking Cdc42 in platelets.
Pleines I, Eckly A, Elvers M, Hagedorn I, Eliautou S, Bender M, Wu X, Lanza F, Gachet C, Brakebusch C, Nieswandt B.
Pleines I, et al.
Blood. 2010 Apr 22;115(16):3364-73. doi: 10.1182/blood-2009-09-242271. Epub 2010 Feb 4.
Blood. 2010.
PMID: 20139097
Free article.
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