Saltar ao contenido
VuFind
English
Deutsch
Español
Français
Italiano
日本語
Nederlands
Português
Português (Brasil)
中文(简体)
中文(繁體)
Türkçe
עברית
Gaeilge
Cymraeg
Ελληνικά
Català
Euskara
Русский
Čeština
Suomi
Svenska
polski
Dansk
slovenščina
اللغة العربية
বাংলা
Galego
Tiếng Việt
Hrvatski
हिंदी
Հայերէն
Українська
Sámegiella
Монгол
Idioma
Todos os campos
Title
Autor
Subject
Número de Clasificación
ISBN/ISSN
Tag
Buscar
Avanzado
Splice-site mutations in the a...
Citar
Text this
Enviar este rexistro por email
Imprimir
Exportar rexistro
Exportar a RefWorks
Exportar a EndNoteWeb
Exportar a EndNote
Permanent link
Splice-site mutations in the achr epsilon subunit gene associated with congenital myasthenic syndrome
Detalles Bibliográficos
Main Authors:
Croxen, R
,
Vincent, A
,
Newsom-Davis, J
,
Beeson, D
Formato:
Journal article
Publicado:
2000
Existencias
Descripción
Títulos similares
Staff View
Títulos similares
Congenital myasthenic syndrome patients due to AChR epsilon subunit mutations
por: Bonifati, D, et al.
Publicado: (2004)
Myasthenia gravis in a woman with congenital AChR deficiency due to epsilon-subunit mutations.
por: Croxen, R, et al.
Publicado: (2002)
Mutation in the AChR ion channel gate underlies a fast channel congenital myasthenic syndrome.
por: Webster, R, et al.
Publicado: (2004)
Structural abnormalities of the AChR caused by mutations underlying congenital myasthenic syndromes.
por: Beeson, D, et al.
Publicado: (2003)
End-plate gamma- and epsilon-subunit mRNA levels in AChR deficiency syndrome due to epsilon-subunit null mutations.
por: Croxen, R, et al.
Publicado: (2001)