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Nmezi B, Giorgio E, Raininko R, et al. Genomic deletions upstream of lamin B1 lead to atypical autosomal dominant leukodystrophy. Neurol Genet. 2019;5(1):e305doi: 10.1212/NXG.0000000000000305.
Nmezi, B., Giorgio, E., Raininko, R., Lehman, A., Spielmann, M., Koenig, M. K., Adejumo, R., Knight, M., Gavrilova, R., Alturkustani, M., Sharma, M., Hammond, R., Gahl, W. A., Toro, C., Brusco, A., & Padiath, Q. S. (2019). Genomic deletions upstream of lamin B1 lead to atypical autosomal dominant leukodystrophy. Neurology. Genetics, 5(1), e305. https://doi.org/10.1212/NXG.0000000000000305
Nmezi, Bruce, et al. "Genomic deletions upstream of lamin B1 lead to atypical autosomal dominant leukodystrophy." Neurology. Genetics vol. 5,1 (2019): e305. doi: https://doi.org/10.1212/NXG.0000000000000305
Nmezi B, Giorgio E, Raininko R, Lehman A, Spielmann M, Koenig MK, Adejumo R, Knight M, Gavrilova R, Alturkustani M, Sharma M, Hammond R, Gahl WA, Toro C, Brusco A, Padiath QS. Genomic deletions upstream of lamin B1 lead to atypical autosomal dominant leukodystrophy. Neurol Genet. 2019 Jan 24;5(1):e305. doi: 10.1212/NXG.0000000000000305. eCollection 2019 Feb. PMID: 30842973; PMCID: PMC6384018.
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