Genomic deletions upstream of lamin B1 lead to atypical autosomal dominant leukodystrophy.
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Neurol Genet. 2019 Jan 24;5(1):e305. doi: 10.1212/NXG.0000000000000305. eCollection 2019 Feb.
Neurol Genet. 2019.
PMID: 30842973
Free PMC article.