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Evidence of Missense Mutations on the Neuregulin 1 Gene Affecting Function of Prepulse Inhibition

โœ Scribed by L. Elliot Hong; Ikwunga Wonodi; O. Colin Stine; Braxton D. Mitchell; Gunvant K. Thaker


Book ID
119197639
Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
199 KB
Volume
63
Category
Article
ISSN
0006-3223

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The forkhead box G1 (FOXG1)gene has recently been associated with the congenital variant of Rett syndrome, and so far 17 mutations have been reported. We screened the coding region in 150 patients affected by postnatal microcephaly, and identified two mutations: the c.326C>T (p.P109L) substitution i