Author:
Albrecht Andrea N.,Kornak Uwe,Böddrich Annett,Süring Kathrin,Robinson Peter N.,Stiege Asita C.,Lurz Rudi,Stricker Sigmar,Wanker Erich E.,Mundlos Stefan
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Reference29 articles.
1. Cummings, C.J. and Zoghbi, H.Y. (2000) Fourteen and counting: unraveling trinucleotide repeat diseases. Hum. Mol. Genet., 6, 909–916.
2. Devys, D., Yvert, G., Lunkes, A., Trottier, Y. and Mandel, J.L. (2001) Pathological mechanisms in polyglutamine expansion diseases. Adv. Exp. Med. Biol., 487, 199–210.
3. Karlin, S., Chen, C., Gentles, A.J. and Cleary, M. (2000) Associations between human disease genes and overlapping gene groups and multiple amino acid runs. Proc. Natl Acad. Sci. USA, 26, 17008–17013.
4. Brown, L.Y. and Brown, S.A. (2004) Alanine tracts: the expanding story of human illness and trinucleotide repeats. Trends Genet., 1, 51–58.
5. Muragaki, Y., Mundlos, S., Upton, J. and Olsen, B.R. (1996) Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13. Science, 272, 548–551.
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