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(2020) A novel variant in C5ORF42 gene is associated with Joubert syndrome. Molecular Biology Reports. pp. 4099-4103. ISSN 0301-4851
(2019) Molecular mechanisms, prevalence, and molecular methods for familial combined hyperlipidemia disease: A review. Journal of Cellular Biochemistry. pp. 8891-8898. ISSN 0730-2312