一般注記出版タイプ: NA
雑誌に発表。PLOS ONE. 12(5):e0177636 (2017); doi:10.1371/journal.pone.0177636.
Thesis
北野 友裕. POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss(次世代シーケンサーにより見出された日本人難聴患者におけるPOU4F3遺伝子変異). 信州大学, 2017, 博士論文.
機関リポジトリ記載の権利情報: © 2017 Kitano et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. / Kitano T, Miyagawa M, Nishio S-y, Moteki H, Oda K, Ohyama K, et al. (2017) POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss. PLoS ONE 12(5): e0177636. https://doi.org/10.1371/journal.pone.0177636
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