Associated Papers
Novel compound heterozygous variants in MARVELD2 causing autosomal recessive hearing loss in two Chinese families.
Shi X et al.
Molecular Genetics & Genomic Medicine, 2024
Case report: A novel nonsense mutation in the MARVELD2 gene causes nonsyndromic hearing loss in a China family.
Huang C et al.
Frontiers in Genetics, 2024
New SNP variants of MARVELD2 (DFNB49) associated with non-syndromic hearing loss in Chinese population.
Zheng J et al.
Journal of Zhejiang University. Science. B, 0
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