| Literature DB >> 22728931 |
Abstract
The molecular mapping of mutations that underlie congenital disorders of monogenic origin can result in both a broader understanding of the molecular basis of the disorder and novel therapeutic insights. Indeed, genotyping patients and then replicating the behavior of the mutant gene products in well-defined biochemical or electrophysiological systems will allow tailoring of therapy to be mutation- and protein sequence-dependent. In this issue of the JCI, Shen and colleagues describe such an approach that identified novel mutations in the α subunit of the nicotinic receptor linked to myasthenia gravis.Entities:
Mesh:
Substances:
Year: 2012 PMID: 22728931 PMCID: PMC3386840 DOI: 10.1172/JCI64409
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808