Sjögren–Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase gene

Author:

Laurenzi Vincenzo De,Rogers Geraldine R.,Hamrock David J.,Marekov Lyuben N.,Steinert Peter M.,Compton John G.,Markova Nelli,Rizzo William B.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Reference22 articles.

1. Sjögren, T. & Larsson, T. Oligophrenia in combination with congenital ichthyosis and spastic disorders. Acta Psychiatr. Neurol. Scand. 32, 1–113 (1957).

2. Jagell, S., Gustavson, K.-H. & Holmgren, G. Sjögren-Larsson syndrome in Sweden: A clinical, genetic and epidemiological study. Clin. Genet. 19, 233–256 (1981).

3. Rizzo, W.B. Sjögren–Larsson syndrome. Semin. Dermatol. 12, 210–218 (1993).

4. Jagell, S. & Heijbel, J. Sjögren–Larsson syndrome: physical and neurological features. Helv. Paediatr. Acta. 37, 519–530 (1982).

5. Rizzo, W.B., Sjögren–Larsson syndrome. In Handbook of Clinical Neurology, (eds Vinken, RJ. & Bruyn, G.W.) (Elsevier, Amsterdam, in the press).

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