dc.contributor.author |
Harzer, Klaus |
de_DE |
dc.date.accessioned |
2013-12-03T10:32:42Z |
|
dc.date.available |
2013-12-03T10:32:42Z |
|
dc.date.issued |
2013 |
de_DE |
dc.identifier.issn |
1096-7192 |
de_DE |
dc.identifier.uri |
http://hdl.handle.net/10900/38557 |
|
dc.language.iso |
en |
en |
dc.publisher |
Academic Press Inc Elsevier Science |
de_DE |
dc.relation.uri |
http://dx.doi.org/10.1016/j.ymgme.2013.04.019 |
de_DE |
dc.rights |
info:eu-repo/semantics/closedAccess |
|
dc.subject.ddc |
570 |
de_DE |
dc.subject.ddc |
610 |
de_DE |
dc.title |
Molecular basis of acid ceramidase deficiency in a neonatal form of Farber disease: Identification of the first large deletion in ASAH1 gene |
de_DE |
dc.type |
Article |
de_DE |
utue.quellen.id |
20130911224530_00388 |
de_DE |
utue.publikation.seiten |
276-281 |
de_DE |
utue.personen.roh |
Alves, Mariana Q. |
de_DE |
utue.personen.roh |
Le Trionnaire, Emmanuelle |
de_DE |
utue.personen.roh |
Ribeiro, Isaura |
de_DE |
utue.personen.roh |
Carpentier, Stephane |
de_DE |
utue.personen.roh |
Harzer, Klaus |
de_DE |
utue.personen.roh |
Levade, Thierry |
de_DE |
utue.personen.roh |
Gil Ribeiro, M. |
de_DE |
dcterms.isPartOf.ZSTitelID |
Molecular Genetics and Metabolism |
de_DE |
dcterms.isPartOf.ZS-Issue |
3 |
de_DE |
dcterms.isPartOf.ZS-Volume |
109 |
de_DE |
utue.fakultaet |
04 Medizinische Fakultät |
de_DE |