Srivastava,A.K., Pispa,J., Hartung,A.J., Du,Y., Ezer,S., Jenks,T., Shimada,T., Pekkanen,M., Mikkola,M., Ko,M.S.H., Thesleff,I., Kere,J., and, Schlessinger,D.
The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains.
Proceedings of the National Academy of Sciences of the United States of America 94:13069-13074 (1997).

Last edited 10.12.2004 by P.N.