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Diagnosis of alpha-1-antitrypsin deficiency by serum protein electrophoresis
Alpha-1-antitrypsin deficiency is a hereditary disease leading to hepatitis and cirrhosis. It is the most common genetic cause of liver disease in children which must inherit the tendency from both parents to develop. It acquires the highest priority in the differential diagnosis in a child with chr...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Springer India
2000
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| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3453954/ https://ncbi.nlm.nih.gov/pubmed/23105261 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/BF02883748 |
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