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pro vyhledávání: '"Abeer M. Eldin"'
Autor:
Lamia H. Selim, Heba Helmy, Heba M. Sharafeldin, Riham A. El-Essawy, Abeer M. Eldin, Fatma A. El-Mougy, Marwa Elsharkawy, Engy A. Mogahed, Hanaa El-Karaksy, Iman Atef Mandour, Sahar A. Sharaf, Dina Hesham Ahmed Soliman
Publikováno v:
Arab Journal of Gastroenterology. 15:114-118
Background and study aims Wilson disease (WD) is an autosomal recessive disorder, caused by defects in copper-transporting P-type adenosine triphosphatase (ATPase) encoded by the ATP7B gene, resulting in the deposition of copper in the liver and brai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::952203cc9228d713fa5726fc3f2a7057
https://doi.org/10.1016/j.ajg.2014.10.005
https://doi.org/10.1016/j.ajg.2014.10.005
