Identification of two recurrent mutations of COL1A1 gene in Chinese Van der Hoeve syndrome patients-Reference-Cited by-同舟云学术

Identification of two recurrent mutations of COL1A1 gene in Chinese Van der Hoeve syndrome patients

Published:2016-04-04 Issue:8 Volume:136 Page:786-791
ISSN:0001-6489
Container-title:Acta Oto-Laryngologica
language:en
Short-container-title:Acta Oto-Laryngologica

Author:

Duan Hong¹²,Yan Zhiqiang³,Lu Yu¹,Cheng Jing⁴,Zhang Di⁵,Yuan Huijun⁴,Han Dongyi¹

Affiliation:

1. Institute of Otolaryngology, Chinese PLA General Hospital, Beijing, PR China;

2. Department of Otolaryngology, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, Inner Mongolia Province, PR China;

3. 97th hospital of PLA (the Chinese People Liberation Army), Xuzhou City, Jiangsu Province, PR China;

4. Medical Genetics Center, Southwest Hospital, Third Military Medical University, Chongqing, PR China;

5. Department of Otorhinolaryngology Head and Neck Surgery, Institute of Otorhinolaryngology, Tianjin First Center Hospital, Tianjin, PR China

Publisher

Informa UK Limited

Subject

Otorhinolaryngology,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.3109/00016489.2016.1159327

Reference19 articles.

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3. Genetic heterogeneity in osteogenesis imperfecta.

4. Osteogenesis Imperfecta Type VI: A Form of Brittle Bone Disease with a Mineralization Defect

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