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Oct 26, 2020 (publication date) through Apr 20, 2024
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Publication Name
World Journal of Clinical Cases
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2307-8960
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Zhou YQ, Wu GS, Kong YM, Zhang XY, Wang CL. New mutation in EPCAM for congenital tufting enteropathy: A case report. World J Clin Cases 2020; 8(20): 4975-4980 [PMID: 33195669 DOI: 10.12998/wjcc.v8.i20.4975] |
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| URL: | https://www.wjgnet.com/1007-9327/full/v8/i20/4975.htm |
| Number | Citing Articles |
| 1 |
Barun Das, Mamata Sivagnanam. Congenital Tufting Enteropathy: Biology, Pathogenesis and Mechanisms. Journal of Clinical Medicine 2020; 10(1): 19 doi: 10.3390/jcm10010019
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| 2 |
Merve Güvenoğlu, Pelin Özlem Şimşek-Kiper, Can Koşukcu, Ekim Z. Taskiran, İnci Nur Saltık-Temizel, Safak Gucer, Eda Utine, Koray Boduroğlu. Homozygous Missense Epithelial Cell Adhesion Molecule Variant in a Patient with Congenital Tufting Enteropathy and Literature Review. Pediatric Gastroenterology, Hepatology & Nutrition 2022; 25(6): 441 doi: 10.5223/pghn.2022.25.6.441
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| 3 |
Hasret Ayyıldız Civan, Coleen Leitner, Iris Östreicher, Anna-Maria Schneider, Malte Cremer, Johannes A. Mayr, Rainer Rossi, Thomas Müller, Andreas R. Janecke. Three Novel EPCAM Variants Causing Tufting Enteropathy in Three Families. Children 2021; 8(6): 503 doi: 10.3390/children8060503
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