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Genomic deletions upstream of lamin B1 lead to atypical autosomal dominant leukodystrophy
OBJECTIVE: Clinical, radiologic, and molecular analysis of patients with genomic deletions upstream of the LMNB1 gene. METHODS: Detailed neurologic, MRI examinations, custom array comparative genomic hybridization (aCGH) analysis, and expression analysis were performed in patients at different clini...
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| Publicat a: | Neurol Genet |
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| Autors principals: | , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Wolters Kluwer
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6384018/ https://ncbi.nlm.nih.gov/pubmed/30842973 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000305 |
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