A mouse model with a frameshift mutation in the nuclear factor I/X (NFIX) gene has phenotypic features of Marshall-Smith syndrome

The nuclear factor <i>I/X</i> (<i>NFIX</i>) gene encodes a ubiquitously expressed transcription factor whose mutations lead to two allelic disorders characterized by developmental, skeletal, and neural abnormalities, namely, Malan syndrome (MAL) and Marshall–Smith syndrome (M...

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Bibliographic Details
Main Authors:	Kooblall, KG, Stevenson, M, Stewart, M, Harris, L, Zalucki, O, Dewhurst, H, Butterfield, N, Leng, H, Hough, TA, Ma, D, Siow, B, Potter, P, Cox, RD, Brown, SDM, Horwood, N, Wright, B, Lockstone, H, Buck, D, Vincent, TL, Hannan, FM, Bassett, JHD, Williams, GR, Lines, KE, Piper, M, Wells, S, Teboul, L, Hennekam, RC, Thakker, RV
Format:	Journal article
Language:	English
Published:	Wiley 2023

A mouse model with a frameshift mutation in the nuclear factor I/X (NFIX) gene has phenotypic features of Marshall-Smith syndrome

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