Novel mutations in TMEM126A causing non-syndromic autosomal recessive optic atrophyN. Weisschuh,M. Synofzik,C. Kernstock, S. Schimpf-Linzenbold,F. Schuettauf,A. Neu, K. KlothEUROPEAN JOURNAL OF HUMAN GENETICS(2019)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