PropertyValue
?:definition
  • Molecular assay reagents intended to identify mutations in the aldehyde dehydrogenase 3 family member A2 (ALDH3A2) gene, located at chromosome 17p11.2, which encodes the protein fatty aldehyde dehydrogenase. Genetic variants at this locus have been associated with Sjogren-Larsson syndrome.
?:hasCUIAnnotation
?:hasGeneratedBy
?:type

Metadata

Anon_0  
expand all