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A novelMYH14mutation in a Chinese family with autosomal dominant nonsyndromic hearing loss

Release Time:2024-04-12 Hits:

Institution:山东省耳鼻喉医院
Journal:BMC MEDICAL GENETICS
Document Code:1B93E16B119945948379035A7BA70DD0
Volume:21
Issue:1
Translation or Not:No
Date of Publication:2020-07

Next One:Lamivudine improves cognitive decline in SAMP8 mice: Integrating in vivo pharmacological evaluation and network pharmacology

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