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1 Ergebnisse
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POU4F3 mutation screening in Japanese hearing loss patients..:
Kitano, Tomohiro
;
Miyagawa, Maiko
;
Nishio, Shin-ya
...
PLOS ONE. 12 (2017) 5 - p. e0177636 , 2017
Link:
https://doi.org/10.1371/journal.pone.0177636
RT Journal T1
POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss
UL https://suche.suub.uni-bremen.de/peid=cr-10.1371_journal.pone.0177636&Exemplar=1&LAN=DE A1 Kitano, Tomohiro A1 Miyagawa, Maiko A1 Nishio, Shin-ya A1 Moteki, Hideaki A1 Oda, Kiyoshi A1 Ohyama, Kenji A1 Miyazaki, Hiromitsu A1 Hidaka, Hiroshi A1 Nakamura, Ken-ichi A1 Murata, Takaaki A1 Matsuoka, Rina A1 Ohta, Yoko A1 Nishiyama, Nobuhiro A1 Kumakawa, Kozo A1 Furutate, Sakiko A1 Iwasaki, Satoshi A1 Yamada, Takechiyo A1 Ohta, Yumi A1 Uehara, Natsumi A1 Noguchi, Yoshihiro A1 Usami, Shin-ichi A1 Malmierca, Manuel S. PB Public Library of Science (PLoS) YR 2017 SN 1932-6203 JF PLOS ONE VO 12 IS 5 SP e0177636 LK http://dx.doi.org/https://doi.org/10.1371/journal.pone.0177636 DO https://doi.org/10.1371/journal.pone.0177636 SF ELIB - SuUB Bremen
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