https://doi.org/10.7490/f1000research.1113554.1
Poster
NOT PEER REVIEWED
Download
metrics
VIEWS
212
 
downloads
14
CITE
How to cite this poster:
Marangi G, Lattante S, Doronzio PN et al. A target NGS approach to clarify the role of genetic variants in ALS pathogenesis [version 1; not peer reviewed]. F1000Research 2016, 5:2883 (poster) (https://doi.org/10.7490/f1000research.1113554.1)
NOTE: it is important to ensure the information in square brackets after the title is included in this citation.

A target NGS approach to clarify the role of genetic variants in ALS pathogenesis

Giuseppe Marangi1, Serena Lattante, Paolo Niccolò Doronzio, Amelia Conte, Katia Patanella, Marcella Zollino, Mario Sabatelli
Author Affiliations
  • Metrics
  • 212 Views
  • 14 Downloads
 
Browse by related subjects
Published 20 Dec 2016

A target NGS approach to clarify the role of genetic variants in ALS pathogenesis

[version 1; not peer reviewed]

Giuseppe Marangi1, Serena Lattante, Paolo Niccolò Doronzio, Amelia Conte, Katia Patanella, Marcella Zollino, Mario Sabatelli
Author Affiliations
1 Università Cattolica del Sacro Cuore, Italy
Presented at
27th International Symposium on ALS/MND 2016
Abstract
Competing Interests

No competing interests were disclosed

Keywords
Amyotrophic lateral sclerosis, ALS, oligogenic
Comments
0 Comments
 
Sign In
If you've forgotten your password, please enter your email address below and we'll send you instructions on how to reset your password.

The email address should be the one you originally registered with F1000.

Email address not valid, please try again

You registered with F1000 via Google, so we cannot reset your password.

To sign in, please click here.

If you still need help with your Google account password, please click here.

You registered with F1000 via Facebook, so we cannot reset your password.

To sign in, please click here.

If you still need help with your Facebook account password, please click here.

Code not correct, please try again
Email us for further assistance.
Server error, please try again.