November 2018

Table of Contents - PeerJ (Medicine Articles)

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November 13, 2018
Family-based whole-exome sequencing identifies novel loss-of-function mutations of FBN1 for Marfan syndrome
Zhening Pu, Haoliang Sun, Junjie Du, Yue Cheng, Keshuai He, Buqing Ni, Weidong Gu, Juncheng Dai, Yongfeng Shao
https://doi.org/10.7717/peerj.5927 PubMed 30479897
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I told my colleagues that PeerJ is a journal where they need to publish if they want their paper to be published quickly and with the strict peer review expected from a good journal.
Sohath Vanegas,
PeerJ Author
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