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March 2014
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otorhinolaryngology
genetics
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March 7, 2014 - Version: 1
Mutation analysis of the
SLC26A4
,
FOXI1
and
KCNJ10
genes in individuals with congenital hearing loss
Lynn M Pique
,
Marie-Luise Brennan
,
Colin J Davidson
,
Frederick Schaefer
,
John Greinwald Jr.
,
Iris Schrijver
https://doi.org/10.7287/peerj.preprints.275v1
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otorhinolaryngology
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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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