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Article

High throughput genetic analysis of congenital myasthenic syndromes using resequencing microarrays.

PloS one - 19 Sept 2007

Denning Lisa, Anderson Jennifer A, Davis Ryan, Gregg Jeffrey P, Kuzdenyi Jennifer, Maselli Ricardo A

Abstract excerpt

BACKGROUND: The use of resequencing microarrays for screening multiple, candidate disease loci is a promising alternative to conventional capillary sequencing. We describe the performance of a custom resequencing microarray for mutational analysis of Congenital Myasthenic Syndromes (CMSs), a grou...

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Share to Myasthenic Syndromes, Congenital
Share to Oligonucleotide Array Sequence Analysis
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 17878953
DOI: 10.1371/journal.pone.0000918
PMCID: PMC1975473

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-17878953-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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