Reply to "Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0"
- PMID: 31502291
- DOI: 10.1002/ana.25597
Reply to "Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0"
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Severe brain involvement in 5q spinal muscular atrophy type 0.Ann Neurol. 2019 Sep;86(3):458-462. doi: 10.1002/ana.25549. Epub 2019 Jul 24. Ann Neurol. 2019. PMID: 31301241
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Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0.Ann Neurol. 2019 Nov;86(5):801-802. doi: 10.1002/ana.25596. Epub 2019 Oct 3. Ann Neurol. 2019. PMID: 31502271 No abstract available.
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Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0.Ann Neurol. 2019 Nov;86(5):801-802. doi: 10.1002/ana.25596. Epub 2019 Oct 3. Ann Neurol. 2019. PMID: 31502271 No abstract available.
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References
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- Mendonça RH, Rocha AJ, Lozano-Arango A, et al. Severe brain involvement in 5q spinal muscular atrophy type 0. Ann Neurol 2019;86:458-462.
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- Rudnik-Schöneborn S, Forkert R, Hahnen E, et al. Clinical spectrum and diagnostic criteria of infantile spinal muscular atrophy: further delineation on the basis of SMN gene deletion findings. Neuropediatrics 1996;27:8-15.
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- Medrano S, Monges S, Gravina LP, et al. Genotype-phenotype correlation of SMN locus genes in spinal muscular atrophy children from Argentina. Eur J Paediatr Neurol 2016;20:910-917.
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- Wang CH, Carter TA, Das K, et al. Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologues. Ann Neurol 1997;42:41-49.
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- Bernal S, Alías L, Barceló MJ, et al. The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor. J Med Genet 2010;47:640-642.
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