High Incidence of Co-Existing Factors Significantly Modifying the Phenotype in Patients with Fabry Disease.Serhat Koca,Leyla Tumer,Ilyas Okur,Yasemin Erten,Sevcan Bakkaloglu,Gursel Biberoglu,Cigdem Kasapkara,Aynur Kucukcongar,Buket Dalgic,Suna Ozhan Oktar,Yusuf Oner,Tuba Atalay,Mustafa Cemri,Bahattin Ciftci, Burcu Topcu,Alev Hasanoglu,Fatih EzguGene（2019）引用 7|浏览47关键词Fabry disease,X-inactivation,Phenotype modifiers,Family screeningAI 理解论文溯源树样例生成溯源树，研究论文发展脉络Chat Paper正在生成论文摘要
