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Cited by in CrossRef
For: Zhang JJ, Wang JQ, Sun MQ, Xu D, Xiao Y, Lu WL, Dong ZY. Alström syndrome with a novel mutation of ALMS1 and Graves’ hyperthyroidism: A case report and review of the literature . World J Clin Cases 2021; 9(13): 3200-3211 [PMID: 33969109 DOI: 10.12998/wjcc.v9.i13.3200]
URL: https://www.wjgnet.com/2307-8960/full/v9/i13/3200.htm
Number Citing Articles
1
Brais Bea-Mascato, Diana Valverde. Genotype–phenotype associations in Alström syndrome: a systematic review and meta-analysisJournal of Medical Genetics 2024; 61(1): 18 doi: 10.1136/jmg-2023-109175
2
Jiaxin Bian, Hongyu Chen, Junhui Sun, Shuai Han, Ming Qi, Qing Pan. Retinol dehydrogenase 12 (RDH12) knock out may cause hyperuricemia phenotype in miceBiochemical and Biophysical Research Communications 2024; 709: 149809 doi: 10.1016/j.bbrc.2024.149809