Genetic screening revealed usher syndrome in a paediatric Chinese patient

Author:

Qu Chunyan1,Liang Fenghe2,Long Qin3,Zhao Min1,Shang Haiqiong4,Fan Lynn5ORCID,Wang Li6ORCID,Yan Denise7,Liu Xuezhong789

Affiliation:

1. China Rehabilitation Research Center for Hearing and Speech Impairment, Beijing, China;

2. Department of Otolaryngology-Head and Neck Surgery, Capital Medical University, Beijing Tongren Hospital, Beijing, China;

3. Department of Ophthalmology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China;

4. Department of Otolaryngology – Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, China;

5. University of Miami, Miami, FL, USA;

6. Institute of Medical Genetics, Henan Provincial People’s Hospital, People’s Hospital of Zhengzhou University, Zhengzhou, China;

7. Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, FL, USA;

8. Dr. John T. Macdonald Department of Human Genetics, University of Miami Miller School of Medicine, Miami, FL, USA;

9. Department of Human Genetics, John P. Hussman Institute for Human Genomics, University of Miami, FL, USA

Funder

National Institutes of Health

National Institute on Deafness and Other Communication Disorders

Publisher

Informa UK Limited

Subject

Speech and Hearing,Otorhinolaryngology

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