Associated Papers
Clinical and Molecular Aspects Associated with Defects in the Transcription Factor POU3F4: A Review.
Bernardinelli E et al.
Biomedicines, 2023
Genetic etiology study of four Chinese families with two nonsyndromic deaf children in succession by targeted next-generation sequencing.
Xiao C et al.
Molecular Genetics & Genomic Medicine, 2021
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