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Celia’s encephalopathy and c.974dupG in BSCL2 gene: a hidden change in a known variant
Celia’s encephalopathy (Progressive Encephalopathy with/without Lipodystrophy, PELD) is a childhood neurodegenerative disorder with a fatal prognosis before the age of 10, due to the variant c.985C>T in the BSCL2 gene that causes a cryptic splicing site leading to skipping of exon 7. For years, d...
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| Pubblicato in: | Neurogenetics |
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| Autori principali: | , , , , , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7288395/ https://ncbi.nlm.nih.gov/pubmed/30903322 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10048-019-00574-5 |
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