Title : A rare case of Sjogren-Larsson syndrome with recurrent pneumonia and asthma.

Pub. Date : 2016 Jun

PMID : 27462357






1 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 An ALDH3A2 gene mutation results in dysfunction of the microsomal enzyme fatty aldehyde dehydrogenase and impaired metabolism and accumulation of leukotriene B4, which is a key molecule and a pro-inflammatory mediator in developing allergic diseases, especially asthma. Leukotriene B4 aldehyde dehydrogenase 3 family member A2 Homo sapiens