Localized TWIST1 and TWIST2 basic domain substitutions cause four distinct human diseases that can be modeled in C. elegans

Twist transcription factors, members of the basic helix-loop-helix family, play crucial roles in mesoderm development in all animals. Humans have two paralogous genes, TWIST1 and TWIST2, and mutations in each gene have been identified in specific craniofacial disorders. Here we describe a new clinic...

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Bibliographic Details
Main Authors:	Kim, S, Twigg, S, Scanlon, V, Chandra, A, Hansen, T, Alsubait, A, Fenwick, A, McGowan, S, Lord, H, Lester, T, Sweeney, E, Weber, A, Cox, H, Wilkie, A, Golden, A, Corsi, A
Format:	Journal article
Published:	Oxford University Press 2017

Localized TWIST1 and TWIST2 basic domain substitutions cause four distinct human diseases that can be modeled in C. elegans

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