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Cited by in CrossRef
For: Mukhopadhya A, Danda S, Huebner A, Chacko A. Mutations of the AAAS gene in an Indian family with Allgrove's syndrome. World J Gastroenterol 2006; 12(29): 4764-4766 [PMID: 16937455 DOI: 10.3748/wjg.v12.i29.4764]
URL: https://www.wjgnet.com/1007-9327/full/v12/i29/4764.htm
Number Citing Articles
1
Yin Zhang, Chun-Di Xu, Abdehaman Zaouche, Wei Cai. Diagnosis and management of esophageal achalasia in children: analysis of 13 casesWorld Journal of Pediatrics 2009; 5(1): 56 doi: 10.1007/s12519-009-0010-9
2
Vijaya Sarathi, Nalini S. Shah. Diseases of DNA RepairAdvances in Experimental Medicine and Biology 2010; 685: 1 doi: 10.1007/978-1-4419-6448-9_1
3
Juan A. Tovar. Pediatric Surgery2012; : 939 doi: 10.1016/B978-0-323-07255-7.00072-6
4
Gabriele Pogliaghi, Biagio Cangiano, Paolo Duminuco, Valeria Vezzoli, Marco Bonomi. Triple-A Syndrome (TAS): An In-Depth Overview on Genetic and Phenotype HeterogeneityProtein & Peptide Letters 2020; 27(12): 1192 doi: 10.2174/0929866527666200613215449
5
Eirini Meimaridou, Julia Kowalczyk, Louise A Metherell. Encyclopedia of Life Sciences2014;  doi: 10.1002/9780470015902.a0025368
6
Philip Morreau. Pediatric Thoracic Surgery2009; : 335 doi: 10.1007/b136543_25
7
Lucila L.K. Elias, AdrianJ.L. Clark. G Protein-Coupled Receptors in Health and Disease, Part AProgress in Molecular Biology and Translational Science 2009; 88: 155 doi: 10.1016/S1877-1173(09)88005-8
8
Michelle A. Veronin, Joseph S. Glavy. The Liver2020; : 94 doi: 10.1002/9781119436812.ch9
9
Kenan Qin, Xiaofei Du, Barry H. Rich. An Alu-mediated rearrangement causing a 3.2kb deletion and a novel two base pair deletion in AAAS gene as the cause of triple A syndromeMolecular Genetics and Metabolism 2007; 92(4): 359 doi: 10.1016/j.ymgme.2007.08.116
10
Jyoti Sanghvi, Ajit Anand Asati, Ravindra Kumar, Angela Huebner. Novel mutations in a patient with triple a syndromeIndian Pediatrics 2015; 52(9): 805 doi: 10.1007/s13312-015-0722-y