Patent AT-E399860-T1: [Translated] MUTATION WITHIN THE CONNEXIN 26 GENE AND RELATION TO PRELINGUAL SYNDROMELESS DEAFNESS AND DETECTION METHODS
Description
A purified polynucleotide having a chain of nucleotides corresponding to a mutated sequence, which in a wild form encodes a polypeptide implicated in hereditary sensory defect wherein said mutated purified polynucleotide presents a mutation responsible for prelingual non-syndromic deafness selected from the group consisting of a specific deletion of at least one nucleotide.
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Access the complete Patent AT-E399860-T1: [Translated] MUTATION WITHIN THE CONNEXIN 26 GENE AND RELATION TO PRELINGUAL SYNDROMELESS DEAFNESS AND DETECTION METHODS on the official website. |
https://pubchem.ncbi.nlm.nih.gov/patent/AT-E399860-T1 |
Tags
- patent
- chemistry
- research
- innovation
- pubchem