Amino acid 118 in the Deafness Causing (DFNA20/26) ACTG1 gene is a Mutational Hot Spot

BACKGROUND: Hearing loss is an economically and socially important cause of human morbidity, affecting 360 million people (over 5% of the world’s population), of whom 32 million are children. Of the estimated minimum of 50% of hereditary hearing loss, non-syndromic hearing loss (NSHL) accounts for m...

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Bibliografiset tiedot
Julkaisussa:Gene Rep
Päätekijät: Wang, Li, Yan, Denise, Qin, Litao, Li, Tao, Liu, Hongjian, Li, Wan, Mittal, Rahul, Yong, Feng, Chapagain, Prem, Liao, Shixiu, Liu, Xuezhong
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2018
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6309262/
https://ncbi.nlm.nih.gov/pubmed/30599039
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.genrep.2018.04.011
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