Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP120780.RAUCwHOTKyrMvUj8dXvqWekLjbQHhuKNXW6ojrfimTwJQ130_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." NP120780.RAUCwHOTKyrMvUj8dXvqWekLjbQHhuKNXW6ojrfimTwJQ130_provenance.
- NP6745.RAKVNeDDX1tM5yy-RW3KKBkApAwwFFKRb1W6MtQwwYJqg130_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." NP6745.RAKVNeDDX1tM5yy-RW3KKBkApAwwFFKRb1W6MtQwwYJqg130_provenance.
- NP183971.RAd27zJAnFaXv7zNKAUCmIFoh4z0khnpipiIUEFdSV3iE130_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." NP183971.RAd27zJAnFaXv7zNKAUCmIFoh4z0khnpipiIUEFdSV3iE130_provenance.
- NP4678.RAXyafpnjlmFUohgV0PSapdlb2CXc7aUs9-2N_1Pe4q5s130_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." NP4678.RAXyafpnjlmFUohgV0PSapdlb2CXc7aUs9-2N_1Pe4q5s130_provenance.
- NP859580.RAz-rkQfLkZkwLpJ6d-jfyigFDrERoOIqgfHxr3oBuaBo130_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." NP859580.RAz-rkQfLkZkwLpJ6d-jfyigFDrERoOIqgfHxr3oBuaBo130_provenance.
- NP4336.RAUe1NEYpUSavy4STH1vga8lYQ2iPLjCmbUUuomEhLJzc130_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." NP4336.RAUe1NEYpUSavy4STH1vga8lYQ2iPLjCmbUUuomEhLJzc130_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.
- NP528973.RAZ4FtkofK31-LYj7crixfZ4SSS3QBKpyi4oJeP63tiR0130_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." NP528973.RAZ4FtkofK31-LYj7crixfZ4SSS3QBKpyi4oJeP63tiR0130_provenance.
- 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." provenance.
- 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." provenance.
- 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." provenance.