HYLS1 protein, human MeSH Supplementary Concept Data 2025

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MeSH Supplementary: HYLS1 protein, human
Unique ID: C505472
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C505472
Entry Term(s): hydrolethalus syndrome 1 protein, human
Registry Numbers: 0
Heading Mapped to: *Proteins
Frequency: 5
Note: mutation in HYLS1 results in hydrolethalus syndrome; RefSeq NM_145014
Source: Hum Mol Genet 2005 Jun 1;14(11):1475-88
Date of Entry: 2005/11/21
Revision Date: 2006/04/19

HYLS1 protein, human Preferred

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