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http://hub.abes.fr/oup/periodical/hmg/2008/volume_17/issue_13/101093hmgddn100/authorship/3
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scienceplus.abes.fr
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http://hub.abes.fr/oup/periodical/hmg/2008/volume_17/issue_13/101093hmgddn100/affiliation/af3
CNRS UMR8104, Institut Cochin
Université Paris Descartes, Faculté de Médecine Cochin-Port-Royal
Université Denis Diderot, Paris VII
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Veitia Reiner
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Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation
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