Associated Papers
MPZL2-a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population.
Zhang L et al.
Bmc Medical Genomics, 2024
A novel MPZL2 c.68delC variant is associated with progressive hearing loss in Chinese population and literature review.
Wang Z et al.
Laryngoscope Investigative Otolaryngology, 2022
The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes-A Comprehensive Study of the GJB2/DFNB1 Region.
Safka Brozkova D et al.
Genes, 2021
[Sequencing of SLC26A4 exons 7 and 8 and hot spot mutation analysis in 1552 moderate to profound sensorineural hearing loss patients in China].
Dai P et al.
Zhonghua Yi Xue Za Zhi, 2007
[The roles of connexin genes in sporadic hearing loss population].
Li QZ et al.
Zhonghua Yi Xue Za Zhi, 2007
[A study on PARKIN gene in three pedigrees with autosomal recessive early-onset Parkinson's disease].
Jin M et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2005
[Screening for mitochondrial DNA mutation in two pedigrees with nonsyndromic inherited sensorineural hearing loss].
Li W et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2002
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