Molecular Basis for Arginase Deficiency in Portugal: a Novel R21X Nonsense Mutation Detected in Six Pediatric Patients with Argininemia

AuthID
 P-001-915
4
Author(s)
Cardoso, ML
·
Martins, E
·
Vilarinho, L
Tipo de Documento
Abstract
Year published
1998
Publicado
in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813
Volume: 6, Páginas: 48-48 (1)
Indexing
Wos®
Publication Identifiers
Wos: WOS:000074522800119
Source Identifiers
ISSN: 1018-4813
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