# Mutations in SEPT9 cause hereditary neuralgic amyotrophy

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/mutations-in-sept9-cause-hereditary-neuralgic-amyotrophy/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Gregor Kuhlenbäumer,Mark Hannibal,Eva Nelis,Anja Schirmacher,Nathalie Verpoorten,Jan Meuleman,Giles D. Watts,Els De Vriendt,Peter Young,Florian Stögbauer,Hartmut Halfter,Joy Irobi,D. Goossens,Jurgen Del‐Favero,Benjamin G Betz,Hyun Hor,G. Kurlemann,Thomas D. Bird,Eila Airaksinen,Tarja Mononen,Adolfo Pou Serradell,J M Prats,Christine Van Broeckhoven,Peter De Jonghe,Vincent Timmerman,E B Ringelstein,Phillip F. Chance |
| Citations | 266 |
| DOI | 10.1038/ng1649 |
| Fields | Biochemistry, Genetics and Molecular Biology,Neuroscience |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W2127839763 |
| PMID | 16186812 |
| Type | article |
| Year | 2005 |

## Paper authors

- [Hartmut Halfter](https://scholariq.org/researchers/hartmut-halfter/)
- [Peter Young](https://scholariq.org/researchers/peter-young/)

## Paper primary topic

- [Connective tissue disorders research](https://scholariq.org/topics/connective-tissue-disorders-research/)

## Paper topics

- [Connective tissue disorders research](https://scholariq.org/topics/connective-tissue-disorders-research/)
- [Ubiquitin and proteasome pathways](https://scholariq.org/topics/ubiquitin-and-proteasome-pathways/)
- [Neurological diseases and metabolism](https://scholariq.org/topics/neurological-diseases-and-metabolism/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.