Pular para o conteúdo
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
Título
Autor
Assunto
Número de Chamada
ISBN/ISSN
Tag
Buscar
Avançada
Effects of epsilon L78P, an ac...
Citar
Enviar por SMS
Enviar por e-mail
Imprimir
Exportar registro
Exportar para RefWorks
Exportar para EndNoteWeb
Exportar para EndNote
Link permanente
Effects of epsilon L78P, an acetylcholine receptor mutation that causes slow channel congenital myasthenic syndrome.
Detalhes bibliográficos
Principais autores:
Shelley, C
,
Brydson, M
,
Beeson, D
,
Colquhoun, D
Formato:
Conference item
Publicado em:
2003
Itens
Descrição
Registros relacionados
Registro fonte
Registros relacionados
Properties of the human muscle nicotinic receptor, and of the slow-channel myasthenic syndrome mutant epsilonL221F, inferred from maximum likelihood fits.
por: Hatton, C, et al.
Publicado em: (2003)
The defect in a slow channel myasthenic syndrome mutant, epsilon L221F
por: Hatton, C, et al.
Publicado em: (2000)
Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes.
por: Croxen, R, et al.
Publicado em: (2002)
Congenital myasthenic syndrome patients due to AChR epsilon subunit mutations
por: Bonifati, D, et al.
Publicado em: (2004)
A Missense Mutation in Epsilon-subunit of Acetylcholine Receptor Causing Autosomal Dominant Slow-channel Congenital Myasthenic Syndrome in a Chinese Family
por: Jia-Ze Tan, et al.
Publicado em: (2016-01-01)