Published September 8, 2021
| Version v1
Dataset
Restricted
Dataset related to article" Missing the pathological expansion in Huntington disease: de novo c.51C>G variant on the expanded allele causing intrafamilial allele dropout"
Authors/Creators
- 1. Fondazione IRCCS Istituto Neurologico Carlo Besta
Description
DATASET CONTAINS Sanger sequencing data of the c.51C>G variant in HTT gene.
Notes
Study supported by grant CP 20/2018 (Care-4NeuroRare) from Fondazione Regionale per la Ricerca Biomedica (FRRB) to F.T, and grant GR-2013-02357821 from the Italian Ministry of Health to Lorenzo Nanetti
Files
Restricted
The record is publicly accessible, but files are restricted. Log in to check if you have access.
Request access
If you would like to request access to these files, please fill out the form below.
You need to satisfy these conditions in order for this request to be accepted:
Users must clarify the intended use of data here uploaded
You are currently not logged in. Do you have an account? Log in here
Additional details
Related works
- Is supplement to
- Journal article: 10.1002/ajmg.a.61973 (DOI)