A novel GLA mutation in a Fabry family with glucose-6-phosphate dehydrogenase deficiency-Reference-Cited by-同舟云学术

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A novel GLA mutation in a Fabry family with glucose-6-phosphate dehydrogenase deficiency

Published:2012 Issue:4 Volume:25 Page:582-585
ISSN:1121-8428
Container-title:Journal of Nephrology
language:en
Short-container-title:JN

Author:

Pisani Antonio,Visciano Bianca,Russo Roberta,Mozzillo Giusi R.,Porto Caterina,De Maggio Ilaria,Russo Roberta,Pontarelli Gianfranco,Villani Guglielmo R.D.,Cianciaruso Bruno,Di Natale Paola

Publisher

SAGE Publications

Subject

Nephrology

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. X Chromosome Deletion in an Iranian Woman with Premature Ovarian Failure and a Mini Review;Urology & Nephrology Open Access Journal;2017-03-03

2. The importance of medical interview with CKD patient in diagnoses of a family with Fabry disease;CEN Case Reports;2014-01-30

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