دورية أكاديمية

Novel pathogenic OCRL mutations and genotype–phenotype analysis of Chinese children affected by oculocerebrorenal syndrome: two cases and a literature review

التفاصيل البيبلوغرافية
العنوان: Novel pathogenic OCRL mutations and genotype–phenotype analysis of Chinese children affected by oculocerebrorenal syndrome: two cases and a literature review
المؤلفون: Zhang, Yu, Deng, Linxia, Chen, Xiaohong, Hu, Yingjie, Chen, Yaxian, Chen, Kang, Zhou, JianhuaAff1
المصدر: BMC Medical Genomics. 14(1)
قاعدة البيانات: Springer Nature Journals
الوصف
تدمد:17558794
DOI:10.1186/s12920-021-01069-9