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

Concepedia

Publication | Closed Access

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

99

Citations

21

References

2002

Year

June M. de la Cruz, Richard N. Bamford, Rebecca D. Burdine, Erich Roessler, James Barkovich, Dian Donnai, Alexander F. Schier, Maximilian Muenke

Cfc DomainDevelopmental BiologyLoss-of-function MutationSomatic VariantGenetic DisorderMendelian DisorderHuman Forebrain DefectsMedicineCell BiologyMolecular Medicine

References

	Year	Citations

Page 1

Page 1