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Deafness- neurosensory- autosomal recessive 47

December 31, 2014

Latest Research

  • <em>PTRH2</em> Gene Variants: Recent Review of the Phenotypic Features and Their Bioinformatics Analysis
  • A clinicopathological study of Alport syndrome and detection of type IV collagen chains in Alport patients
  • A mouse model for human deafness DFNB22 reveals that hearing impairment is due to a loss of inner hair cell stimulation
  • A novel connexin 26 mutation associated with autosomal recessive sensorineural deafness
  • A Novel Mutation of SLC19A2 in a Chinese Zhuang Ethnic Family with Thiamine-Responsive Megaloblastic Anemia
More Research
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