Reply to “Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0”-Reference-Cited by-同舟云学术

Reply to “Global Central Nervous System Atrophy in Spinal Muscular Atrophy Type 0”

Published:2019-10-03 Issue:5 Volume:86 Page:803-803
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol

Author:

Mendonça Rodrigo H.¹,Rocha Antônio J.²,Lozano‐Arango Andres³^ORCID,Diaz Astry B.³,Castiglioni Claudia⁴^ORCID,Silva André M. S.¹^ORCID,Reed Umbertina C.¹,Kulikowski Leslie⁵,Paramonov Ida⁶,Cuscó Ivon⁶,Tizzano Eduardo F.⁶^ORCID,Zanoteli Edmar¹^ORCID

Affiliation:

1. Department of NeurologyFaculdade de Medicina da Universidade de São Paulo (FMUSP) São Paulo Brazil

2. Neuroradiology SectionHigh Diagnostic Excellence (DASA Group) São Paulo Brazil

3. Hernan Henriquez Aravena Regional Hospital Temuco Chile

4. Department of Pediatric NeurologyClínica Las Condes Santiago Chile

5. Department of PathologyFaculdade de Medicina da Universidade de São Paulo (FMUSP) São Paulo Brazil

6. Department of Clinical and Molecular Genetics, Valle Hebron Universitary HospitalMedicine Genetics Group, Valle Hebron Research Institute Barcelona Spain

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ana.25597

Reference5 articles.

1. Severe brain involvement in 5q spinal muscular atrophy type 0

2. Clinical Spectrum and Diagnostic Criteria of Infantile Spinal Muscular Atrophy: Further Delineation on the Basis of SMN Gene Deletion Findings

3. Genotype–phenotype correlation of SMN locus genes in spinal muscular atrophy children from Argentina

4. Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologues

5. The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor