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[1] . A novelMYH14mutation in a Chinese family with autosomal dominant nonsyndromic hearing loss. BMC MEDICAL GENETICS, 21, 2020.
[2] 李明. Lamivudine improves cognitive decline in SAMP8 mice: Integrating in vivo pharmacological evaluation and network pharmacology. journal of cellular and molecular med..., 25, 8490, 2021.
[3] 白晓卉. Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families (vol 2020, pg 9, 2020). BioMed Research International, 2020, 2020.

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