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1 Ergebnisse
1
Novel ACTG1 mutations in patients identified by massively p..:
Miyajima, Hiroki
;
Moteki, Hideaki
;
Day, Timothy
...
Scientific Reports. 10 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1038/s41598-020-63690-5
RT Journal T1
Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing loss
UL https://suche.suub.uni-bremen.de/peid=cr-10.1038_s41598-020-63690-5&Exemplar=1&LAN=DE A1 Miyajima, Hiroki A1 Moteki, Hideaki A1 Day, Timothy A1 Nishio, Shin-ya A1 Murata, Takaaki A1 Ikezono, Tetsuo A1 Takeda, Hidehiko A1 Abe, Satoko A1 Iwasaki, Satoshi A1 Takahashi, Masahiro A1 Naito, Yasushi A1 Yamazaki, Hiroshi A1 Kanda, Yukihiko A1 Kitajiri, Shin-ichiro A1 Usami, Shin-ichi PB Springer Science and Business Media LLC YR 2020 SN 2045-2322 JF Scientific Reports VO 10 IS 1 LK http://dx.doi.org/https://doi.org/10.1038/s41598-020-63690-5 DO https://doi.org/10.1038/s41598-020-63690-5 SF ELIB - SuUB Bremen
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