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Lysosomal Acid Lipase Deficiency: Report of Five Cases across the Age Spectrum
Lysosomal acid lipase (LAL) deficiency is an autosomal recessive lysosomal storage disorder caused by mutations in the LIPA gene that leads to premature organ damage and mortality. We present retrospective data from medical records of 5 Brazilian patients, showing the broad clinical spectrum of the...
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| Pubblicato in: | Case Rep Pediatr |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Hindawi
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5828415/ https://ncbi.nlm.nih.gov/pubmed/29527374 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2018/4375434 |
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