Fabry Disease
Fabry disease is a rare genetic disease involving a deficiency of an enzyme. A decrease in the enzyme activity leads to a selective suffering of specific anatomic and functional structures resulting in heteromorphic clinical signs that increase the difficulty of early diagnosis. Knowing and identify...
| الحاوية / القاعدة: | Romanian Journal of Neurology |
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| المؤلفون الرئيسيون: | , , , , |
| التنسيق: | مقال |
| اللغة: | الإنجليزية |
| منشور في: |
Amaltea Medical Publishing House
2018-12-01
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| الموضوعات: | |
| الوصول للمادة أونلاين: | https://rjn.com.ro/articles/2018.4/RJN_2018_4_Art-05.pdf |