LETTER TO THE EDITOR
Mutations of NOS1 and MLN regulatory sequences are a potential cause of infantile hypertrophic pyloric stenosis
Submission date: 2016-06-26
Acceptance date: 2016-08-24
Publication date: 2016-09-08
Arch Med Sci Civil Dis 2016;1(1):79-80
TOPICS
REFERENCES (5)
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MacMahon B. The continuing enigma of pyloric stenosis of infancy: a review. Epidemiology 2006; 17: 195-201.
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Chung E, Curtis D, Chen G, et al. Genetic evidence for the neuronal nitric oxide synthase gene (NOS1) as a susceptibility locus for infantile pyloric stenosis. Am J Hum Genet 1996; 58: 363-70.
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Svenningsson A, Söderhäll C, Persson S, et al. Genome-wide linkage analysis in families with infantile hypertrophic pyloric stenosis indicates novel susceptibility loci. J Hum Genet 2012; 57: 115-21.
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Zhang C, Li WH, Krainer AR, Zhang MQ. RNA landscape of evolution for optimal exon and intron discrimination. Proc Natl Acad Sci USA 2008; 105: 5797-802.
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Saur D, Vanderwinden JM, Seidler B, Schmid RM, De Laet MH, Allescher HD. Single-nucleotide promoter polymorphism alters transcription of neuronal nitric oxide synthase exon 1c in infantile hypertrophic pyloric stenosis. Proc Natl Acad Sci USA 2004; 101: 1662-7.
| ISSN: | 2451-0637 |
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