Variant c.394C>T in FGF3 is a recurrent cause of profound congenital deafness in Slovak Roma Maria Giertlova, Martin Mistrik, Petra Drencakova, Veronika Lopackova, Renata Zemjarova Mezenska, Katarina Cokasova, Michaela Urminska, Zuzana Zbonakova,Viktor Stranecky,Lenka NoskovaEUROPEAN JOURNAL OF HUMAN GENETICS(2023)引用 0|浏览6暂无评分AI 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