TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities.
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Wiszniewski W, et al. Among authors: madduri ns.
Am J Hum Genet. 2013 Aug 8;93(2):197-210. doi: 10.1016/j.ajhg.2013.05.027. Epub 2013 Jun 27.
Am J Hum Genet. 2013.
PMID: 23810381
Free PMC article.