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Decision letter for "Novel TRRAP mutation causes autosomal dominant non-syndromic hearing loss"
Mapping Intimacies
◽
10.1111/cge.13590/v3/decision1
◽
2019
◽
Keyword(s):
Hearing Loss
◽
Autosomal Dominant
◽
Syndromic Hearing Loss
Download Full-text
Related Documents
Cited By
References
Review for "Novel TRRAP mutation causes autosomal dominant non-syndromic hearing loss"
10.1111/cge.13590/v1/review1
◽
2019
◽
Keyword(s):
Hearing Loss
◽
Autosomal Dominant
◽
Syndromic Hearing Loss
Download Full-text
Case Report: Novel Heterozygous DFNA5 Splicing Variant Responsible for Autosomal Dominant Non-syndromic Hearing Loss in a Chinese Family
Frontiers in Genetics
◽
10.3389/fgene.2020.569284
◽
2020
◽
Vol 11
◽
Author(s):
Xi Chen
◽
Bao-Long Jia
◽
Mei-Hui Li
◽
Yuan Lyu
◽
Cai-Xia Liu
Keyword(s):
Hearing Loss
◽
Case Report
◽
Autosomal Dominant
◽
Chinese Family
◽
Splicing Variant
◽
Syndromic Hearing Loss
Download Full-text
Identification of a Novel Copy Number Variation of EYA4 Causing Autosomal Dominant Non-Syndromic Hearing Loss
Otology & Neurotology
◽
10.1097/mao.0000000000003169
◽
2021
◽
Vol Publish Ahead of Print
◽
Author(s):
Takashi Ishino
◽
Yui Ogawa
◽
Toru Sonoyama
◽
Takayuki Taruya
◽
Takashi Kono
◽
...
Keyword(s):
Hearing Loss
◽
Copy Number Variation
◽
Copy Number
◽
Autosomal Dominant
◽
Number Variation
◽
Syndromic Hearing Loss
Download Full-text
Review for "Novel TRRAP mutation causes autosomal dominant non-syndromic hearing loss"
10.1111/cge.13590/v3/review1
◽
2019
◽
Author(s):
A. Giese
Keyword(s):
Hearing Loss
◽
Autosomal Dominant
◽
Syndromic Hearing Loss
Download Full-text
Author response for "Novel TRRAP mutation causes autosomal dominant non-syndromic hearing loss"
10.1111/cge.13590/v3/response1
◽
2019
◽
Author(s):
Wenjun Xia
◽
Jiongjiong Hu
◽
Jing Ma
◽
Jianbo Huang
◽
Xu Wang
◽
...
Keyword(s):
Hearing Loss
◽
Autosomal Dominant
◽
Author Response
◽
Syndromic Hearing Loss
Download Full-text
Review for "Novel TRRAP mutation causes autosomal dominant non-syndromic hearing loss"
10.1111/cge.13590/v1/review2
◽
2019
◽
Author(s):
A. Giese
Keyword(s):
Hearing Loss
◽
Autosomal Dominant
◽
Syndromic Hearing Loss
Download Full-text
Decision letter for "Novel TRRAP mutation causes autosomal dominant non-syndromic hearing loss"
10.1111/cge.13590/v1/decision1
◽
2019
◽
Keyword(s):
Hearing Loss
◽
Autosomal Dominant
◽
Syndromic Hearing Loss
Download Full-text
A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3
Journal of Medical Genetics
◽
10.1136/jmg.2003.010702
◽
2004
◽
Vol 41
(1)
◽
pp. 11-13
◽
Cited By ~ 16
Author(s):
R L Snoeckx
Keyword(s):
Hearing Loss
◽
Autosomal Dominant
◽
Syndromic Hearing Loss
◽
Chromosome 6P21.3
Download Full-text
Screening of the SLC17A8 gene as a causative factor for autosomal dominant non-syndromic hearing loss in Koreans
BMC Medical Genetics
◽
10.1186/s12881-016-0269-3
◽
2016
◽
Vol 17
(1)
◽
Cited By ~ 10
Author(s):
Nari Ryu
◽
Borum Sagong
◽
Hong-Joon Park
◽
Min-A Kim
◽
Kyu-Yup Lee
◽
...
Keyword(s):
Hearing Loss
◽
Autosomal Dominant
◽
Causative Factor
◽
Syndromic Hearing Loss
Download Full-text
A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6
Human Molecular Genetics
◽
10.1093/hmg/5.6.853
◽
1996
◽
Vol 5
(6)
◽
pp. 853-856
◽
Cited By ~ 45
Author(s):
M. O'Neill
Keyword(s):
Hearing Loss
◽
Autosomal Dominant
◽
Late Onset
◽
Chromosome 6
◽
Syndromic Hearing Loss
Download Full-text
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