Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia

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Item Type:	Article
Title:	Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia
Creators Name:	Slaugenhaupt, S.A., Blumenfeld, A., Gill, S.P., Leyne, M., Mull, J., Cuajungco, M.P., Liebert, C.B., Chadwick, B., Idelson, M., Reznik, L., Robbins, C.M., Makalowska, I., Brownstein, M.J., Krappmann, D., Scheidereit, C., Maayan, C., Axelrod, F.B. and Gusella, J.F.
Source:	American Journal of Human Genetics
ISSN:	0002-9297
Publisher:	University of Chicago Press
Volume:	68
Page Range:	598-605
Date:	1 January 2001
Official Publication:	http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1274473&rendertype=abstract
PubMed:	View item in PubMed

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