Decision letter for "Novel TRRAP mutation causes autosomal dominant non-syndromic hearing loss"

2019 ◽  
Keyword(s):  
Hearing Loss ◽  
Autosomal Dominant ◽  
Syndromic Hearing Loss

Identification of a Novel Copy Number Variation of EYA4 Causing Autosomal Dominant Non-Syndromic Hearing Loss

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

Author response for "Novel TRRAP mutation causes autosomal dominant non-syndromic hearing loss"

2019 ◽  
Author(s):  
Wenjun Xia ◽  
Jiongjiong Hu ◽  
Jing Ma ◽  
Jianbo Huang ◽  
Xu Wang ◽  
...  
Keyword(s):  
Hearing Loss ◽  
Autosomal Dominant ◽  
Author Response ◽  
Syndromic Hearing Loss

scholarly journals Screening of the SLC17A8 gene as a causative factor for autosomal dominant non-syndromic hearing loss in Koreans

2016 ◽  
Vol 17 (1) ◽  
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
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