Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1

By Saleem Ramsey A.  

Human Molecular Genetics, Vol. 12, Iss. 22, 2003-11 ,pp. : 2993-3005

Oxford University Press

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FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome

By Kriederman Benjamin M.  

Human Molecular Genetics, Vol. 12, Iss. 10, 2003-05 ,pp. : 1179-1185

Oxford University Press

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

By Beysen Diane   Moumn Lara   Veitia Reiner   Peters Hartmut   Leroy Bart P.   De Paepe Anne   De Baere Elfride  

Human Molecular Genetics, Vol. 17, Iss. 13, 2008-07 ,pp. : 2030-2038

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Truncating mutations in FOXC2 cause multiple lymphedema syndromes

By Finegold D.N.  

Human Molecular Genetics, Vol. 10, Iss. 11, 2001-05 ,pp. : 1185-1189

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In-Frame Deletion and Missense Mutations of the C-Terminal Helicase Domain of SMARCA2 in Three Patients with Nicolaides-Baraitser Syndrome

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Karger

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