A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects.
de la Cruz JM; Bamford RN; Burdine RD; Roessler E; Barkovich AJ; Donnai D; Schier AF; Muenke M; Human Genetics, 2002, vol. 110, issue 5, p 422, ISSN 03406717. ISBN 03406717.

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