Author:
Rodríguez Cruz Pedro M.,Hughes Imelda,Manzur Adnan,Munot Pinki,Ramdas Sithara,Wright Ronnie,Breen Catherine,Pitt Mathew,Pagnamenta Alistair T.,Taylor Jenny C.,Palace Jacqueline,Beeson David
Funder
National Institute for Health Research
Medical Research Council
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
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4. Synaptotagmin 2 mutations cause an autosomal-dominant form of lambert-eaton myasthenic syndrome and nonprogressive motor neuropathy;Herrmann;Am J Hum Genet,2014
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