A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss-Reference-Cited by-同舟云学术

A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss

Published:2010-05 Issue:5 Volume:86 Page:797-804
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Sırmacı Aslı,Erbek Seyra,Price Justin,Huang Mingqian,Duman Duygu,Cengiz F. Başak,Bademci Güney,Tokgöz-Yılmaz Suna,Hişmi Burcu,Özdağ Hilal,Öztürk Banu,Kulaksızoğlu Sevsen,Yıldırım Erkan,Kokotas Haris,Grigoriadou Maria,Petersen Michael B.,Shahin Hashem,Kanaan Moien,King Mary-Claire,Chen Zheng-Yi,Blanton Susan H.,Liu Xue Z.,Zuchner Stephan,Akar Nejat,Tekin Mustafa

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference27 articles.

1. Newborn hearing screening—A silent revolution;Morton;N. Engl. J. Med.,2006

2. Genetic epidemiology of hearing impairment;Morton;Ann. N Y Acad. Sci.,1991

3. Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey;Tekin;Eur. J. Pediatr.,2003

4. Genetic epidemiological studies of congenital/prelingual deafness in turkey: Population structure and mating type are major determinants of mutation identification;Tekin;Am. J. Med. Genet. A.,2007

5. GRR: Graphical representation of relationship errors;Abecasis;Bioinformatics,2001

Cited by 52 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A Consolidated Understanding of the Contribution of Redox Dysregulation in the Development of Hearing Impairment;Antioxidants;2024-05-13

2. Novel maternal duplication of 6p22.3-p25.3 with subtelomeric 6p25.3 deletion: new clinical findings and genotype–phenotype correlations;Molecular Cytogenetics;2023-06-11

3. Analysis of genetic dominance in the UK Biobank;Science;2023-03-31

4. Absence of Serpinb6a causes progressive hair cell apoptosis and hearing loss in mice;Journal of Genetics and Genomics;2023-02

5. ARNSHL gene identification: past, present and future;Molecular Genetics and Genomics;2022-07-23