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  • A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects.

A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects.

Author List
de la Cruz JM, Bamford RN, Burdine RD, Roessler E, Barkovich AJ, Donnai D, Schier AF, Muenke M
Publication
Human genetics
Publication ID (Profile URL)
https://researcherprofiles.org/profile/55028443
Publication Year
2002
PubMed ID
12073012