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- NP214850.RAW2FA0zvhOlbGiotdBkELPY5ZZc_qTri6qxGKUyDX_oA130_assertion type Assertion NP214850.RAW2FA0zvhOlbGiotdBkELPY5ZZc_qTri6qxGKUyDX_oA130_head.
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- NP214850.RAW2FA0zvhOlbGiotdBkELPY5ZZc_qTri6qxGKUyDX_oA130_assertion wasDerivedFrom lhgdn-20090331 NP214850.RAW2FA0zvhOlbGiotdBkELPY5ZZc_qTri6qxGKUyDX_oA130_provenance.
- NP214850.RAW2FA0zvhOlbGiotdBkELPY5ZZc_qTri6qxGKUyDX_oA130_assertion SIO_000772 16385458 NP214850.RAW2FA0zvhOlbGiotdBkELPY5ZZc_qTri6qxGKUyDX_oA130_provenance.
- NP214850.RAW2FA0zvhOlbGiotdBkELPY5ZZc_qTri6qxGKUyDX_oA130_assertion evidence source_evidence_literature NP214850.RAW2FA0zvhOlbGiotdBkELPY5ZZc_qTri6qxGKUyDX_oA130_provenance.
- NP214850.RAW2FA0zvhOlbGiotdBkELPY5ZZc_qTri6qxGKUyDX_oA130_assertion description "[Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP214850.RAW2FA0zvhOlbGiotdBkELPY5ZZc_qTri6qxGKUyDX_oA130_provenance.