Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation

Title
Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation
Authors
Keywords
-
Journal
HUMAN MOLECULAR GENETICS
Volume 17, Issue 13, Pages 2030-2038
Publisher
Oxford University Press (OUP)
Online
2008-03-28
DOI
10.1093/hmg/ddn100

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