M Brydson

Author PubWeight™ 9.32^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	Properties of the human muscle nicotinic receptor, and of the slow-channel myasthenic syndrome mutant epsilonL221F, inferred from maximum likelihood fits.	J Physiol	2003	1.99
2	Primary structure of the human muscle acetylcholine receptor. cDNA cloning of the gamma and epsilon subunits.	Eur J Biochem	1993	1.14
3	Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes.	Neurology	2002	1.04
4	Acetylcholine receptor delta subunit mutations underlie a fast-channel myasthenic syndrome and arthrogryposis multiplex congenita.	J Clin Invest	2001	1.02
5	Nucleotide sequence of human muscle acetylcholine receptor beta-subunit.	Nucleic Acids Res	1989	0.95
6	End-plate gamma- and epsilon-subunit mRNA levels in AChR deficiency syndrome due to epsilon-subunit null mutations.	Brain	2001	0.86
7	Voluntary partial retraction of: Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes.	Neurology	2009	0.81
8	Mutation in the AChR ion channel gate underlies a fast channel congenital myasthenic syndrome.	Neurology	2004	0.81
9	cDNA and genomic clones encoding the human muscle acetylcholine receptor.	Ann N Y Acad Sci	1993	0.79