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Novel human pathological mutations. Gene symbol: HMBS. Disease: porphyria, acute intermittent.
Di Pierro, E; Besana, V; Brancaleoni, V; Ausenda, S; Lonati, P; Cappellini, M D.
Affiliation
  • Di Pierro E; Department of Internal Medicine- University of Milan, Centro Anemie Congenite-Maggiore Policlinico, Mangiagalli and Regina Elena Hospital IRCCS. Via F.Sforza, 35 20122 Milan, Italy. elena.dipierro@unimi.it
Hum Genet ; 122(3-4): 417, 2007 Nov.
Article de En | MEDLINE | ID: mdl-18350657
Recherche sur Google
Collection: 01-internacional Base de données: MEDLINE Sujet principal: Hydroxymethylbilane synthase / Porphyrie aigüe intermittente Limites: Humans Langue: En Journal: Hum Genet Année: 2007 Type de document: Article Pays d'affiliation: Italie
Recherche sur Google
Collection: 01-internacional Base de données: MEDLINE Sujet principal: Hydroxymethylbilane synthase / Porphyrie aigüe intermittente Limites: Humans Langue: En Journal: Hum Genet Année: 2007 Type de document: Article Pays d'affiliation: Italie