Concurrent OPA1 mutation and chromosome 3q deletion leading to Behr syndrome: a case report
OPA1基因突变合并3q染色体缺失导致贝赫尔综合征:病例报告
期刊:BMC Pediatr
影响因子:2.000
doi:10.1186/s12887-020-02309-0.
Ting Zeng ,Linyan Liao ,Yi Guo ,Xuxu Liu ,Xiaobo Xiong ,Yu Zhang ,Shi Cen ,Honghui Li ,Shuzhang Wei