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] |
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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-analysis. Journal of Medical Genetics 2024; 61(1): 18 doi: 10.1136/jmg-2023-109175
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2 |
Jiaxin Bian, Hongyu Chen, Junhui Sun, Shuai Han, Ming Qi, Qing Pan. Retinol dehydrogenase 12 (RDH12) knock out may cause hyperuricemia phenotype in mice. Biochemical and Biophysical Research Communications 2024; 709: 149809 doi: 10.1016/j.bbrc.2024.149809
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