# Frequent genes in rare diseases: panel‐based next generation sequencing to disclose causal mutations in hereditary neuropathies

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/frequent-genes-in-rare-diseases-panel-based-next-generation-sequencing-to/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Maike F. Dohrn,Nicola Glöckle,Lejla Mulahasanovic,Corina Heller,Julia Mohr,Christine Bauer,Erik Riesch,Andrea C. Becker,Florian Battke,Konstanze Hörtnagel,Thorsten Hornemann,Saranya Suriyanarayanan,Markus Blankenburg,Jörg B. Schulz,Kristl G. Claeys,Burkhard Gess,István Katona,A. Ferbert,Debora Vittore,Alexander Grimm,Stefan Wolking,Lüdger Schöls,Holger Lerche,Georg Christoph Korenke,Dirk Fischer,Bertold Schrank,Urania Kotzaeridou,Gerhard Kurlemann,Bianca Dräger,Anja Schirmacher,Peter Young,Beate Schlotter‐Weigel,Saskia Biskup |
| Citations | 80 |
| DOI | 10.1111/jnc.14217 |
| Fields | Biochemistry, Genetics and Molecular Biology,Neuroscience |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W2754226141 |
| PMID | 28902413 |
| Type | article |
| Year | 2017 |

## Paper authors

- [Maike F. Dohrn](https://scholariq.org/researchers/maike-f-dohrn/)
- [Burkhard Gess](https://scholariq.org/researchers/burkhard-gess/)

## Paper primary topic

- [Hereditary Neurological Disorders](https://scholariq.org/topics/hereditary-neurological-disorders/)

## Paper topics

- [Hereditary Neurological Disorders](https://scholariq.org/topics/hereditary-neurological-disorders/)
- [Endoplasmic Reticulum Stress and Disease](https://scholariq.org/topics/endoplasmic-reticulum-stress-and-disease/)
- [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.