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November 2018
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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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