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Genomic variants in the coding region of neuronal nitric oxide synthase (NOS1) in infantile hypertrophic pyloric stenosis

✍ Scribed by Alexandre Serra; Katrin Schuchardt; Jon Genuneit; Clothilde Leriche; Guido Fitze


Book ID
116689190
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
179 KB
Volume
46
Category
Article
ISSN
0022-3468

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Variants in the neuronal nitric oxide sy
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## Abstract Sixty percent of the patients with restless legs syndrome (RLS) report a positive family history. To date five loci have been mapped on chromosome 12q, 14q, 9p, 2q, and 20p (RLS1‐5) but no gene has been identified so far. To identify genes related to RLS, we performed a three‐stage asso