Whole‐exome sequencing identified a novel homozygous ASPH frameshift variant causing Traboulsi syndrome in a Chinese family
Whole‐exome sequencing identified a novel homozygous ASPH frameshift variant causing Traboulsi syndrome in a Chinese family
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DOI：
10.1002/mgg3.1553
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发表时间：
2020
影响因子：
2
通讯作者：
Hong Luo
中科院分区：
文献类型：
--
作者：
Cheng Lei;Ting Guo;Shuizi Ding;Hong Peng;Liyan Liao;Zhiping Tan;Hong Luo
