# Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/novel-loss-of-function-mutations-in-npr2-cause-acromesomelic-dysplasia-maroteaux/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Jing Wu,Mengru Wang,Zhouyang Jiao,Bing-Hua Dou,Bo Li,Jianjiang Zhang,Haohao Zhang,Yue Sun,Xin Tu,Xiangdong Kong,Ying Bai |
| Citations | 26 |
| DOI | 10.3389/fgene.2022.823861 |
| Fields | Biochemistry, Genetics and Molecular Biology |
| Open Access | true |
| OA Status | gold |
| OA URL | https://doi.org/10.3389/fgene.2022.823861 |
| OpenAlex ID | https://openalex.org/W4220941002 |
| PMID | 35368703 |
| Type | article |
| Year | 2022 |

## Paper authors

- [Jianjiang Zhang](https://scholariq.org/researchers/jianjiang-zhang/)

## Paper primary topic

- [Ubiquitin and proteasome pathways](https://scholariq.org/topics/ubiquitin-and-proteasome-pathways/)

## Paper topics

- [Ubiquitin and proteasome pathways](https://scholariq.org/topics/ubiquitin-and-proteasome-pathways/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Connective tissue disorders research](https://scholariq.org/topics/connective-tissue-disorders-research/)

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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.