Old Web
English
Sign In
Acemap
>
Paper
>
Two mutations, one family: C9orf72 and SQSTM1 in neurodegenerative diseases
Two mutations, one family: C9orf72 and SQSTM1 in neurodegenerative diseases
2019
Patricia L. Henegan
Kevin Chysna
Kate Essad
Elijah W. Stommel
Keywords:
Physical therapy
Diabetes mellitus
C9orf72
Bioinformatics
Medicine
Frontotemporal dementia
Amyotrophic lateral sclerosis
Correction
Source
Cite
Save
Machine Reading By IdeaReader
11
References
1
Citations
NaN
KQI
[]