Zobrazeno 1 - 2
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pro vyhledávání: '"Catherine Hartog"'
Autor:
Richard L.M. Faull, Mauro Delorenzi, Linda Anne Elliston, Doris C. V. Thu, Darlene R. Goldstein, Francois Collin, Andrew D. Strand, Catherine Hartog, Aaron K. Aragaki, Charles Kooperberg, Ruth Luthi-Carter, Sarah J. Augood, James M. Olson, Lesley Jones, Alexandre Kuhn, Peter Holmans, Anne B. Young, Nancy S. Wexler, Zane R. Hollingsworth, Angela Hodges, Beth J. Synek, Gareth Hughes, Thierry Sengstag
Huntington's disease (HD) pathology is well understood at a histological level but a comprehensive molecular analysis of the effect of the disease in the human brain has not previously been available. To elucidate the molecular phenotype of HD on a g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86bdbf86a814ac64fbe03bf038300822
http://doc.rero.ch/record/301565/files/ddl013.pdf
http://doc.rero.ch/record/301565/files/ddl013.pdf
Publikováno v:
Human Mutation. 14:87-87
Hunter syndrome is a rare, X-linked, recessively inherited disease affecting approximately 1 in 132,000 males. The disease is caused by the inability to degrade dermatan sulphate and heparan sulphate due to mutations in the iduronate-2-sulphatase gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5ba4eefb65a70a21f823338e3a52559
https://doi.org/10.1002/(sici)1098-1004(1999)14:1<87::aid-humu14>3.0.co
https://doi.org/10.1002/(sici)1098-1004(1999)14:1<87::aid-humu14>3.0.co
