A rare co-occurrence of duchenne muscular dystrophy, congenital adrenal hypoplasia and glycerol kinase deficiency due to Xp21 contiguous gene deletion syndrome: case report
杜氏肌营养不良症、先天性肾上腺发育不全和甘油激酶缺乏症罕见共存病例报告（Xp21邻近基因缺失综合征）：病例报告
期刊:BMC Endocrine Disorders
影响因子:3.3
doi:10.1186/s12902-021-00876-6
Rathnasiri, Asanka; Senarathne, Udara; Arunath, Visvalingam; Hoole, Thabitha; Kumarasiri, Ishara; Muthukumarana, Oshanie; Jasinge, Eresha; Mettananda, Sachith
