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1 Ergebnisse
1
Mutational Spectrum and Clinical Features of Patients with ..:
Karuna Maekawa
;
Shin-ya Nishio
;
Satoko Abe
...
Human Genomics and Genetic Diseases. , 2019
Link:
https://doi.org/10.3390/genes10100735
RT Journal T1
Mutational Spectrum and Clinical Features of Patients with LOXHD1 Variants Identified in an 8074 Hearing Loss Patient Cohort
UL https://suche.suub.uni-bremen.de/peid=base-ftmdpi:oai:mdpi.com:_2073-4425_10_10_735_&Exemplar=1&LAN=DE A1 Karuna Maekawa A1 Shin-ya Nishio A1 Satoko Abe A1 Shin-ichi Goto A1 Yohei Honkura A1 Satoshi Iwasaki A1 Yukihiko Kanda A1 Yumiko Kobayashi A1 Shin-ichiro Oka A1 Mayuri Okami A1 Chie Oshikawa A1 Naoko Sakuma A1 Hajime Sano A1 Masayuki Shirakura A1 Natsumi Uehara A1 Shin-ichi Usami PB Multidisciplinary Digital Publishing Institute YR 2019 K1 LOXHD1 K1 non-syndromic hearing loss K1 DFNB77 K1 recurrent variation K1 haplotype analysis K1 cochlear implantation JF Human Genomics and Genetic Diseases LK http://dx.doi.org/https://doi.org/10.3390/genes10100735 DO https://doi.org/10.3390/genes10100735 SF ELIB - SuUB Bremen
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