Fabry disease: from clinical manifestations to molecular mechanisms
Identifieur interne : 000662 ( France/Analysis ); précédent : 000661; suivant : 000663Fabry disease: from clinical manifestations to molecular mechanisms
Auteurs : K. Azibi [France] ; C. Heltianu ; C. Caillaud [France] ; J. Manicom [France] ; Jp Puech [France] ; A. Kahn [France] ; L. Poenaru [France]Source :
- Acta Pædiatrica [ 0803-5253 ] ; 2002-11.
Url:
DOI: 10.1111/j.1651-2227.2002.tb03129.x
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 002365
- to stream Istex, to step Curation: 002365
- to stream Istex, to step Checkpoint: 002662
- to stream Main, to step Merge: 009B00
- to stream Main, to step Curation: 009719
- to stream Main, to step Exploration: 009719
- to stream France, to step Extraction: 000662
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ISTEX:4D578A3819D30719E0830326E3F4A05976F865B9Le document en format XML
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