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Cited by in CrossRef
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]
URL: https://www.wjgnet.com/2307-8960/full/v8/i20/4975.htm
Number Citing Articles
1
A. A. Kovaleva, I. A. Leonova, A. A. Sukhotskaya, A. P. Smorodin, V. G. Bairov, N. M. Anichkov, E. Yu. Kalinina, Z. V. Davydova, E. P. Fedotova. The difficult path to diagnosis. A case of tufting enteropathyExperimental and Clinical Gastroenterology 2024; (1): 99 doi: 10.31146/1682-8658-ecg-221-1-99-104
2
Barun Das, Mamata Sivagnanam. Congenital Tufting Enteropathy: Biology, Pathogenesis and MechanismsJournal of Clinical Medicine 2020; 10(1): 19 doi: 10.3390/jcm10010019
3
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 ReviewPediatric Gastroenterology, Hepatology & Nutrition 2022; 25(6): 441 doi: 10.5223/pghn.2022.25.6.441
4
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 FamiliesChildren 2021; 8(6): 503 doi: 10.3390/children8060503