Energy utilization of induced pluripotent stem cell-derived cardiomyocyte in Fabry disease

Author:

Chou Shih-Jie,Yu Wen-Chung,Chang Yuh-Lih,Chen Wen-Yeh,Chang Wei-Chao,Chien Yueh,Yen Jiin-Cherng,Liu Yung-Yang,Chen Shih-Jen,Wang Chien-Ying,Chen Yu-Han,Niu Dau-Ming,Lin Shing-Jong,Chen Jaw-Wen,Chiou Shih-Hwa,Leu Hsin-Bang

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference30 articles.

1. α-Galactosidase A deficiency: Fabry disease;Eng,2001

2. Fabry disease: incidence of the common later-onset α-galactosidase A IVS4+919G→A mutation in Taiwanese newborns–superiority of DNA-based to enzyme-based newborn screening for common mutations;Chien;Mol. Med.,2012

3. Gaucher disease and Fabry disease: new markers and insights in pathophysiology for two distinct glycosphingolipidoses;Ferraz;Biochim. Biophys. Acta,1841

4. Characterization of alpha-galactosidase isoenzymes in normal and Fabry human-Chinese Hamster somatic cell hybrids;Hamers;Hum. Genet.,1977

5. Structural organization of the human alpha-galactosidase A gene: further evidence for the absence of a 3′ untranslated region;Bishop;Proc. Natl. Acad. Sci. U. S. A.,1988

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