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Cited by in CrossRef
For: Xu HJ, Wen GD. Mixed porokeratosis with a novel mevalonate kinase gene mutation: A case report. World J Clin Cases 2022; 10(14): 4528-4534 [PMID: 35663074 DOI: 10.12998/wjcc.v10.i14.4528]
URL: https://www.wjgnet.com/2307-8960/full/v10/i14/4528.htm
Number Citing Articles
1
Qin Mei, Fengling Xing, Yue Yin, Chengda Yuan. Case Report: A Novel MVK Missense Mutation in the Sporadic Porokeratosis Ptychotropica in ChinaClinical, Cosmetic and Investigational Dermatology 2023; : 1325 doi: 10.2147/CCID.S408016
2
Paweł Pietkiewicz, Katarzyna Korecka, Natalia Salwowska, Ihor Kohut, Adarsha Adhikari, Monika Bowszyc-Dmochowska, Anna Pogorzelska-Antkowiak, Cristian Navarrete-Dechent. Porokeratoses—A Comprehensive Review on the Genetics and Metabolomics, Imaging Methods and Management of Common Clinical VariantsMetabolites 2023; 13(12): 1176 doi: 10.3390/metabo13121176
3
Xiuping Wang, Xiaoliang Ouyang, Deng Zhang, Yunxia Zhu, Liang Wu, Zhen Xiao, Simin Yu, Wei Li, Chunming Li. Two Novel and Three Recurrent Mutations in the Mevalonate Pathway Genes in Chinese Patients with PorokeratosisClinical, Cosmetic and Investigational Dermatology 2024; : 191 doi: 10.2147/CCID.S444985