Sjögren-Larsson syndrome: molecular genetics and biochemical pathogenesis of fatty aldehyde dehydrogenase deficiency. | Mol Genet Metab;90(1): 1-9, 2007 Jan. | MEDLINE

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Sjögren-Larsson syndrome: molecular genetics and biochemical pathogenesis of fatty aldehyde dehydrogenase deficiency.

Rizzo, William B.

Affiliation

Rizzo WB; Department of Pediatrics, University of Nebraska Medical Center, 985456 Nebraska Medical Center, Omaha, NE 68164-5456, USA. wrizzo@unmc.edu

Mol Genet Metab ; 90(1): 1-9, 2007 Jan.

Article in En | MEDLINE | ID: mdl-16996289

Subject(s)

Aldehyde Oxidoreductases/deficiency; Aldehyde Oxidoreductases/genetics; Sjogren-Larsson Syndrome/enzymology; Sjogren-Larsson Syndrome/genetics; Aldehyde Oxidoreductases/metabolism; Humans; Lipid Metabolism; Sjogren-Larsson Syndrome/diagnosis; Sjogren-Larsson Syndrome/therapy

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Full text: 1 Database: MEDLINE Main subject: Sjogren-Larsson Syndrome / Aldehyde Oxidoreductases Type of study: Diagnostic_studies / Etiology_studies Limits: Humans Language: En Year: 2007 Type: Article

Search on Google

Full text: 1 Database: MEDLINE Main subject: Sjogren-Larsson Syndrome / Aldehyde Oxidoreductases Type of study: Diagnostic_studies / Etiology_studies Limits: Humans Language: En Year: 2007 Type: Article