Genetics of Hirschsprung’s disease
Genetics of Hirschsprung’s disease
About this item
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Publisher
Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title
Language
English
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Publication information
Publisher
Berlin/Heidelberg: Springer Berlin Heidelberg
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Scope and Contents
Contents
Hirschsprung’s disease (HSCR) is a classical model of enteric neuropathy, occurring in approximately 2–2.8 in 10,000 newborns. It is the commonest form of congenital bowel obstruction and is characterized by the absence of enteric ganglia in distal colon. Recent advances in genome-wide association analysis (GWAS) and next generation sequencing (NGS...
Alternative Titles
Full title
Genetics of Hirschsprung’s disease
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Record Identifier
TN_cdi_proquest_miscellaneous_2774268152
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2774268152
Other Identifiers
ISSN
1437-9813,0179-0358
E-ISSN
1437-9813
DOI
10.1007/s00383-022-05358-x
