Spectrum of AGL mutations in Chinese patients with glycogen storage disease type III: identification of 31 novel mutations.

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🔗 View Article (PMID 26984562)

Published in J Hum Genet on March 17, 2016

Authors

Chaoxia Lu¹, Zhengqing Qiu², Miao Sun¹^,3, Wei Wang², Min Wei², Xue Zhang¹

Author Affiliations

1: McKusick-Zhang Center for Genetic Medicine, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and School of Basic Medcine, Peking Union Medical College, Beijing, China.
2: Department of Pediatrics, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
3: Institute for Fetology, the First Affiliated Hospital of Soochow University, Suzhou, China.

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