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Duplication and deletion upstream of LMNB1 in autosomal dominant adult-onset leukodystrophy
OBJECTIVE: To characterize the genetic and clinical features of patients with autosomal dominant adult-onset demyelinating leukodystrophy (ADLD) carrying duplication and deletion upstream of lamin B1 (LMNB1). METHODS: Ninety-three patients with adult-onset leukoencephalopathy of unknown etiology wer...
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| Pubblicato in: | Neurol Genet |
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| Autori principali: | , , , , , , , , , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Wolters Kluwer
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6340331/ https://ncbi.nlm.nih.gov/pubmed/30697589 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000292 |
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