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SNX8: A candidate gene for 7p22 cardiac malformations including tetralogy of fallot.
Am J Med Genet A. 2014 Feb;164A(2):554-6. doi: 10.1002/ajmg.a.36242. Epub 2013 Dec 5.
Am J Med Genet A. 2014.
PMID: 24311514
No abstract available.
Correspondence regarding SNX8 haploinsufficiency and its potential for cardiac anomalies including tetralogy of Fallot.
Vanzo RJ, Martin MM, Sdano MR, Teta K, South ST.
Vanzo RJ, et al. Among authors: teta k.
Am J Med Genet A. 2014 Aug;164A(8):2136-7. doi: 10.1002/ajmg.a.36572. Epub 2014 Apr 14.
Am J Med Genet A. 2014.
PMID: 24733602
No abstract available.
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