Analysis of MYO15A variation in children with DFNB3
Objective: To analyze the genetic and clinical characteristics of MYO15A variants associated non-syndromic autosomal recessive deafness3 (DFNB3). Methods: The hearing test and high-throughput sequencing data of 108 families with non-syndromic hearing loss, who visited the Center of Genetics and Pren...
Description complète
Détails bibliographiques
| Publié dans: | Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 58(2020), 10 vom: 02. Okt., Seite 818-823
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| Auteur principal: |
Ren, S M
(Auteur) |
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| Autres auteurs: |
Wu, Q H,
Jiao, Z H,
Chen, Y B,
Chen, C,
Kong, X D,
Qin, Z B |
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| Format: | Article en ligne
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| Langue: | Chinese |
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| Publié: |
2020
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| Accès à la collection: | Zhonghua er ke za zhi = Chinese journal of pediatrics
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| Sujets: | Journal Article
Deafness
Genes
Phenotype
MYO15A protein, human
Myosins
EC 3.6.4.1 |
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