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Are There Neurological Symptoms in Type 1 of Gaucher Disease?
OBJECTIVE: Gaucher disease (GD) is a rare inborn error of metabolism, classified as a lipid storage disorders. This disease is caused by a deficiency in glucocerebrosidase enzyme. It has been classified according to the presence or absence of neurological symptoms into the following types: type 1 no...
Uloženo v:
| Vydáno v: | Iran J Child Neurol |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Shahid Beheshti University of Medical Sciences
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5904744/ https://ncbi.nlm.nih.gov/pubmed/29696051 |
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