Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies-Reference-Cited by-同舟云学术

Filamin B Loss-of-Function Mutation in Dimerization Domain Causes Autosomal-Recessive Spondylocarpotarsal Synostosis Syndrome with Rib Anomalies

Author:

Yang Chi-Fan¹,Wang Chung-Hsing²³,Siong H'ng Weng¹,Chang Chun-Ping¹,Lin Wei-De⁴⁵,Chen Yuan-Tsong¹,Wu Jer-Yuarn¹,Tsai Fuu-Jen⁴⁶⁷⁸

Affiliation:

1. Institute of Biomedical Sciences, Academia Sinica; Taipei Taiwan

2. Department of Genetics and Metabolism; Children's Hospital of China Medical University; Taichung Taiwan

3. School of Medicine; China Medical University; Taichung Taiwan

4. Department of Medical Genetics; China Medical University Hospital; Taichung Taiwan

5. School of Post Baccalaureate Chinese Medicine; China Medical University; Taichung Taiwan

6. Department of Medical Research; China Medical University Hospital; Taichung Taiwan

7. School of Chinese Medicine; China Medical University; Taichung Taiwan

8. Division of Pediatric Genetics, Endocrinology & Metabolism; China Medical University Children's Hospital; Taichung Taiwan

Funder

Academia Sinica Genomic Medicine Multicenter Study

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

Reference51 articles.

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