MeSH Browser

MeSH Supplementary: MIRN96 microRNA, human
Unique ID: C541492
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C541492
Entry Term(s): hsa-mir-96, human; miR-96, human; microRNA-96, human
Registry Numbers: 0
Heading Mapped to: *MicroRNAs
Frequency: 208
Note: mutations associated with nonsyndromic progressive hearing loss; GenBank AF480534
Source: Nat Genet 2009 May;41(5):609-13
Date of Entry: 2009/06/23
Revision Date: 2009/06/23

Concept UI: M0536762
Registry Numbers: 0
Terms: MIRN96 microRNA, human Preferred Term
Term UI T753268
Date06/23/2009
LexicalTag NON
ThesaurusID NLM (2009); hsa-mir-96, human
Term UI T753269
Date06/23/2009
LexicalTag NON
ThesaurusID NLM (2009); miR-96, human
Term UI T753270
Date06/23/2009
LexicalTag NON
ThesaurusID NLM (2009); microRNA-96, human
Term UI T753271
Date06/23/2009
LexicalTag NON
ThesaurusID NLM (2009)

MIRN96 microRNA, human MeSH Supplementary Concept Data 2025