Published March 29, 2021
| Version v1
Dataset
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Data related to article " Sorting Rare ALS Genetic Variants by Targeted Re-Sequencing Panel in Italian Patients: OPTN, VCP, and SQSTM1 Variants Account for 3% of Rare Genetic Forms"
Authors/Creators
- 1. Fondazione IRCCS - Istituto Neurologico Carlo Besta di Milano
Description
Genetic analysis with a multi-gene panel including 46 genes in 213 consecutive patients with sporadic or familial ALS
Notes
Study supported by Fondazione Regionale per la Ricerca Biomedica (Regione Lombardia, Grant FRRB 2015-0023 ) and the Italian Ministry of Health (Grant RF 2013-02355764).
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Additional details
Related works
- Is supplement to
- Journal article: 10.3390/jcm9020412 (DOI)