Autosomal dominant hereditary spastic paraplegia: Novel mutations in the <it>REEP1 </it>gene (SPG31)
<p>Abstract</p> <p>Background</p> <p>Mutations in the <it>SPG4 </it>gene (spastin) and in the <it>SPG3A </it>gene (atlastin) account for the majority of 'pure' autosomal dominant form of hereditary spastic paraplegia (HSP). Recently, mu...
Saved in:
Main Authors: | Epplen Joerg T (Author), Arning Larissa (Author), Schlang Katharina J (Author), Stemmler Susanne (Author) |
---|---|
Format: | Book |
Published: |
BMC,
2008-07-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Cold temperature improves mobility and survival in Drosophila models of autosomal-dominant hereditary spastic paraplegia (AD-HSP)
by: Sally L. Baxter, et al.
Published: (2014) -
A patient-derived stem cell model of hereditary spastic paraplegia with SPAST mutations
by: Greger Abrahamsen, et al.
Published: (2013) -
A patient-derived stem cell model of hereditary spastic paraplegia with SPAST mutations
by: Greger Abrahamsen, et al.
Published: (2015) -
A novel SPAST gene mutation identified in a Chinese family with hereditary spastic paraplegia
by: Weiwei Yu, et al.
Published: (2020) -
Neuraxial anesthesia for a laboring patient with hereditary spastic paraplegia: A case report
by: Joshua Falescky, et al.
Published: (2022)