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CLMP is required for intestinal development, and loss-of-function mutations cause congenital short-bowel syndrome.
Gastroenterology. 2012 Mar;142(3):453-462.e3. doi: 10.1053/j.gastro.2011.11.038. Epub 2011 Dec 7.
Gastroenterology. 2012.
PMID: 22155368
Identification of Variants in RET and IHH Pathway Members in a Large Family With History of Hirschsprung Disease.
Sribudiani Y, Chauhan RK, Alves MM, Petrova L, Brosens E, Harrison C, Wabbersen T, de Graaf BM, Rügenbrink T, Burzynski G, Brouwer RWW, van IJcken WFJ, Maas SM, de Klein A, Osinga J, Eggen BJL, Burns AJ, Brooks AS, Shepherd IT, Hofstra RMW.
Sribudiani Y, et al.
Gastroenterology. 2018 Jul;155(1):118-129.e6. doi: 10.1053/j.gastro.2018.03.034. Epub 2018 Mar 28.
Gastroenterology. 2018.
PMID: 29601828
Free article.
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In vivo visualization of the development of the enteric nervous system using a Tg(-8.3bphox2b:Kaede) transgenic zebrafish.
Harrison C, Wabbersen T, Shepherd IT.
Harrison C, et al.
Genesis. 2014 Dec;52(12):985-90. doi: 10.1002/dvg.22826. Epub 2014 Nov 4.
Genesis. 2014.
PMID: 25264359
Free PMC article.
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