Galloway-Mowat syndrome in Taiwan: OSGEP mutation and unique clinical phenotype

Lin, Pei-Yi; Tseng, Min-Hua; Zenker, Martin; Rao, Jia; Hildebrandt, Friedhelm; Lin, Shih-Hua; Lin, Chun-Chen; Chang, Jui-Hsing; Hsu, Chyong-Hsin; Lee, Ming-Dar; Lin, Shuan-Pei; Tsai, Jeng-Daw

期刊名称Orphanet Journal of Rare Diseases
作者Lin, Pei-Yi; Tseng, Min-Hua; Zenker, Martin; Rao, Jia; Hildebrandt, Friedhelm; Lin, Shih-Hua; Lin, Chun-Chen; Chang, Jui-Hsing; Hsu, Chyong-Hsin; Lee, Ming-Dar; Lin, Shuan-Pei; Tsai, Jeng-Daw
卷第13卷
期第1期
电子ISSN1750-1172
文件大小4157.74KB
发表时间2018-12
DOI10.1186/s13023-018-0961-9

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Galloway-Mowat syndrome in Taiwan: OSGEP mutation and unique clinical phenotype