Clinical, biochemical, and genetic aspects of Sjögren-Larsson syndrome

Author:

Cho K.H.1ORCID,Shim S.H.2,Kim M.1ORCID

Affiliation:

1. Department of Rehabilitation Medicine; CHA Bundang Medical Center, CHA University; Seongnam Korea

2. Genetics Laboratory, Fertility Center, CHA Gangnam Medical Center; CHA University; Seoul Korea

Funder

Basic Science Research Program from Korea National Research Foundation

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference61 articles.

1. Oligophrenia in combination with congenital ichthyosis and spastic disorders; a clinical and genetic study;Sjogren;Acta Psychiatr Neurol Scand Suppl,1957

2. Specific changes in the fundus typical for the Sjogren-Larsson syndrome. An ophthalmological study of 35 patients;Jagell;Acta Ophthalmol (Copenh),1980

3. A case of Sjogren-Larsson syndrome;Lee;Korean J Pediatr,1994

4. Sjogren-Larsson syndrome: molecular genetics and biochemical pathogenesis of fatty aldehyde dehydrogenase deficiency;Rizzo;Mol Genet Metab,2007

5. Sjogren-larsson syndrome: a study of clinical symptoms and dermatological treatment in 34 Swedish patients;Ganemo;Acta Derm Venereol,2009

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