信州大学(Shinshu university)博士(医学)雑誌に発表。BMC MEDICAL GENETICS. 14():95 (2013); doi:10.1186/1471-2350-14-95.Thesis岩佐 陽一郎. OTOF mutation screening in Japanese severe to profound recessive hearing loss patients (常染色体劣性遺伝形式をとる日本人高度~重度難聴患者におけるOTOF遺伝子変異スクリーニング). 信州大学, 2013, 博士論文.doctoral thesi
International audienceBackgroundMutations in OTOF gene, encoding otoferlin, cause DFNB9 deafness and...
The OTOF gene encoding otoferlin is associated with auditory neuropathy (AN), a type of non-syndromi...
Abstract Background While auditory neuropathy spectrum disorder (ANSD) is a heterogeneous disorder a...
The OTOF gene (Locus: DFNB9), encoding otoferlin, is reported to be one of the major causes of non-s...
The OTOF gene (Locus: DFNB9), encoding otoferlin, is reported to be one of the major causes of non-s...
信州大学(Shinshu university)博士(医学)雑誌に発表。PLOS ONE. 11(9):e0162230 (2016); doi:10.1371/journal.pone.016223...
博士(医学)信州大学(Shinshu university)Doctoral医学乙第1225号雑誌に発表。PLOS ONE. 13(3):e0193359 (2018); doi:10.1371/jo...
Although etiological studies have shown genetic disorders to be a common cause of congenital/early-o...
Sensorineural hearing loss is one of the most common neurosensory disorders in humans. The incidence...
<div><p>A variant in a transcription factor gene, <i>POU4F3</i>, is responsible for autosomal domina...
Autosomal recessive nonsyndromic hearing impairment (NSHI) is a heterogeneous condition, for which 5...
Mutations in the OTOF gene have been found to be common causes of auditory neuropathy (AN) in Caucas...
A variant in a transcription factor gene, POU4F3, is responsible for autosomal dominant nonsyndromic...
Although etiological studies have shown genetic disorders to be a common cause of congenital/early-o...
Autosomal recessive nonsyndromic hearing impairment (NSHI) is a heterogeneous condition, for which 5...
International audienceBackgroundMutations in OTOF gene, encoding otoferlin, cause DFNB9 deafness and...
The OTOF gene encoding otoferlin is associated with auditory neuropathy (AN), a type of non-syndromi...
Abstract Background While auditory neuropathy spectrum disorder (ANSD) is a heterogeneous disorder a...
The OTOF gene (Locus: DFNB9), encoding otoferlin, is reported to be one of the major causes of non-s...
The OTOF gene (Locus: DFNB9), encoding otoferlin, is reported to be one of the major causes of non-s...
信州大学(Shinshu university)博士(医学)雑誌に発表。PLOS ONE. 11(9):e0162230 (2016); doi:10.1371/journal.pone.016223...
博士(医学)信州大学(Shinshu university)Doctoral医学乙第1225号雑誌に発表。PLOS ONE. 13(3):e0193359 (2018); doi:10.1371/jo...
Although etiological studies have shown genetic disorders to be a common cause of congenital/early-o...
Sensorineural hearing loss is one of the most common neurosensory disorders in humans. The incidence...
<div><p>A variant in a transcription factor gene, <i>POU4F3</i>, is responsible for autosomal domina...
Autosomal recessive nonsyndromic hearing impairment (NSHI) is a heterogeneous condition, for which 5...
Mutations in the OTOF gene have been found to be common causes of auditory neuropathy (AN) in Caucas...
A variant in a transcription factor gene, POU4F3, is responsible for autosomal dominant nonsyndromic...
Although etiological studies have shown genetic disorders to be a common cause of congenital/early-o...
Autosomal recessive nonsyndromic hearing impairment (NSHI) is a heterogeneous condition, for which 5...
International audienceBackgroundMutations in OTOF gene, encoding otoferlin, cause DFNB9 deafness and...
The OTOF gene encoding otoferlin is associated with auditory neuropathy (AN), a type of non-syndromi...
Abstract Background While auditory neuropathy spectrum disorder (ANSD) is a heterogeneous disorder a...