# Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/usher-syndrome-1d-and-nonsyndromic-autosomal-recessive-deafness-dfnb12-are/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Julie M. Bork,Linda Peters,Saima Riazuddin,Steven L. Bernstein,Zubair M. Ahmed,Seth Ness,Robert C. Polomeno,Arabandi Ramesh,Melvin D. Schloss,C.R. Srikumari Srisailpathy,Sigrid Wayne,Susan Bellman,Dilip Desmukh,Zahoor Ahmed,Shaheen N. Khan,Vazken M. Der Kaloustian,X. Cindy Li,Anil K. Lalwani,Sheikh Riazuddin,Maria Bitner‐Glindzicz,Walter E. Nance,Xue Zhong Liu,Graeme Wistow,Richard J. Smith,Andrew J. Griffith,Edward R. Wilcox,Thomas B. Friedman,Robert J. Morell |
| Citations | 558 |
| DOI | 10.1086/316954 |
| Fields | Biochemistry, Genetics and Molecular Biology,Neuroscience |
| Open Access | true |
| OA Status | bronze |
| OA URL | http://www.cell.com/article/S0002929707624690/pdf |
| OpenAlex ID | https://openalex.org/W2038502254 |
| PMID | 11090341 |
| Type | article |
| Year | 2001 |

## Paper authors

- [Richard J. Smith](https://scholariq.org/researchers/richard-j-smith/)

## Paper primary topic

- [Hearing, Cochlea, Tinnitus, Genetics](https://scholariq.org/topics/hearing-cochlea-tinnitus-genetics/)

## Paper topics

- [Hearing, Cochlea, Tinnitus, Genetics](https://scholariq.org/topics/hearing-cochlea-tinnitus-genetics/)
- [Ion Channels and Receptors](https://scholariq.org/topics/ion-channels-and-receptors/)
- [Connexins and lens biology](https://scholariq.org/topics/connexins-and-lens-biology/)

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