TY  - GEN
AU  - Kitano,Tomohiro
AU  - Miyagawa,Maiko
AU  - Nishio,Shin-Ya
AU  - Moteki,Hideaki
AU  - Oda,Kiyoshi
AU  - Ohyama,Kenji
AU  - Miyazaki,Hiromitsu
AU  - Hidaka,Hiroshi
AU  - Nakamura,Ken-Ichi
AU  - Murata,Takaaki
AU  - Matsuoka,Rina
AU  - Ohta,Yoko
AU  - Nishiyama,Nobuhiro
AU  - Kumakawa,Kozo
AU  - Furutate,Sakiko
AU  - Iwasaki,Satoshi
AU  - Yamada,Takechiyo
AU  - Ohta,Yumi
AU  - Uehara,Natsumi
AU  - Noguchi,Yoshihiro
AU  - Usami,Shin-Ichi
TI  - POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss
SN  - 1932-6203
PY  - 2017///0915
KW  - Adolescent
KW  - Adult
KW  - Aged
KW  - Asian People
KW  - genetics
KW  - Child
KW  - Child, Preschool
KW  - Codon, Nonsense
KW  - DNA
KW  - chemistry
KW  - Female
KW  - Frameshift Mutation
KW  - Gene Frequency
KW  - Hearing Loss, Sensorineural
KW  - High-Throughput Nucleotide Sequencing
KW  - Homeodomain Proteins
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Japan
KW  - Male
KW  - Middle Aged
KW  - Mutation, Missense
KW  - Pedigree
KW  - Polymorphism, Genetic
KW  - Sequence Analysis, DNA
KW  - Transcription Factor Brn-3C
KW  - Young Adult
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1371/journal.pone.0177636
ER  -