LymphedemaV1, Main, Exploration, bibRecord, 009135

Fabry disease: molecular studies in Italian patients and X inactivation analysis in manifesting carriers

Identifieur interne : 009135 ( Main/Exploration ); précédent : 009134; suivant : 009136

Fabry disease: molecular studies in Italian patients and X inactivation analysis in manifesting carriers

Auteurs : A. Morrone [Italie] ; C. Cavicchi [Italie] ; T. Bardelli [Italie] ; D. Antuzzi [Italie] ; R. Parini [Italie] ; M. Di Rocco [Italie] ; S. Feriozzi [Italie] ; O. Gabrielli [Italie] ; R. Barone [Italie] ; G. Pistone [Italie] ; C. Spisni [Italie] ; R. Ricci [Italie] ; E. Zammarchi [Italie]

Source :

Journal of Medical Genetics [ 0022-2593 ] ; 2003-08.

RBID : ISTEX:05C6331AD9677E5C251C0822B546DF4898ACDAB9

English descriptors

KwdEn :
- Fabry disease, GLA deficiency, X inactivation, α-galactosidase deficiency.

Url:

DOI: 10.1136/jmg.40.8.e103

Affiliations:

Le document en format XML

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Serveur d'exploration sur le lymphœdème

Fabry disease: molecular studies in Italian patients and X inactivation analysis in manifesting carriers

Fabry disease: molecular studies in Italian patients and X inactivation analysis in manifesting carriers

Source :

English descriptors

Links toward previous steps (curation, corpus...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

	Serveur d'exploration sur le lymphœdème
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