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The cover image is based on the Original Article Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1 by Mao Lin et al., https://doi.org/10.1002/mgg3.1023 .

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Published in:Molecular genetics & genomic medicine 2020-01, Vol.8 (1)
Main Authors: Lin, Mao, Liu, Zhenlei, Liu, Gang, Zhao, Sen, Li, Chao, Chen, Weisheng, Coban Akdemir, Zeynep, Lin, Jiachen, Song, Xiaofei, Wang, Shengru, Xu, Qiming, Zhao, Yanxue, Wang, Lianlei, Zhang, Yuanqiang, Yan, Zihui, Liu, Sen, Liu, Jiaqi, Chen, Yixin, Zuo, Yuzhi, Yang, Xu, Sun, Tianshu, Yang, Xin‐Zhuang, Niu, Yuchen, Li, Xiaoxin, You, Wesley, Qiu, Bintao, Ding, Chen, Liu, Pengfei, Zhang, Shuyang, Carvalho, Claudia M. B., Posey, Jennifer E., Qiu, Guixing, Lupski, James R., Wu, Zhihong, Zhang, Jianguo, Wu, Nan
Format: Article
Language:English
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Summary:The cover image is based on the Original Article Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1 by Mao Lin et al., https://doi.org/10.1002/mgg3.1023 .
ISSN:2324-9269
DOI:10.1002/mgg3.1158