Skip to content
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
Jezik
Vsa polja
Naslov
Avtor
Tema
Signatura
ISBN/ISSN
Oznaka
Išči
Napredno
Effects of epsilon L78P, an ac...
Citiraj
Pošljite SMS
Pošljite email
Natisni
Izvozi zadetek
Izvozi v RefWorks
Izvozi v EndNoteWeb
Izvozi v EndNote
Permanent link
Effects of epsilon L78P, an acetylcholine receptor mutation that causes slow channel congenital myasthenic syndrome.
Bibliografske podrobnosti
Main Authors:
Shelley, C
,
Brydson, M
,
Beeson, D
,
Colquhoun, D
Format:
Conference item
Izdano:
2003
Zaloga
Opis
Podobne knjige/članki
Knjižničarski pogled
Podobne knjige/članki
Properties of the human muscle nicotinic receptor, and of the slow-channel myasthenic syndrome mutant epsilonL221F, inferred from maximum likelihood fits.
od: Hatton, C, et al.
Izdano: (2003)
The defect in a slow channel myasthenic syndrome mutant, epsilon L221F
od: Hatton, C, et al.
Izdano: (2000)
Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes.
od: Croxen, R, et al.
Izdano: (2002)
Congenital myasthenic syndrome patients due to AChR epsilon subunit mutations
od: Bonifati, D, et al.
Izdano: (2004)
A Missense Mutation in Epsilon-subunit of Acetylcholine Receptor Causing Autosomal Dominant Slow-channel Congenital Myasthenic Syndrome in a Chinese Family
od: Jia-Ze Tan, et al.
Izdano: (2016-01-01)