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A newly identified chromosomal microdeletion and an N-box mutation of the AChR{epsilon} gene cause a congenital myasthenic syndrome
Oxford University Press | 2002| -
Expression of foetal type acetylcholine receptor is restricted to type 1 muscle fibres in human neuromuscular disorders
Oxford University Press | 2002| -
Genome-wide association study in essential tremor identifies three new loci
Oxford University Press | 2016|
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