Galloway-Mowat syndrome in Taiwan: OSGEP mutation and...

Orphanet Journal of Rare Diseases 2018 / 12 Vol. 13; Iss. 1

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
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Volume:
13
Language:
english
Journal:
Orphanet Journal of Rare Diseases
DOI:
10.1186/s13023-018-0961-9
Date:
December, 2018
File:
PDF, 4.06 MB
english, 2018
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