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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Gene Rep |
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| Κύριοι συγγραφείς: | , , , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2018
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| Θέματα: | |
| Διαθέσιμο Online: | 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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