A novel point mutation of the FALDH gene in a Japa...[J Invest Dermatol. 2000] - PubMed Result

SearchDatabase nameforSearch term

Advanced Search

Your browser version may not work well with NCBI's Web applications. More information here...

Display Show

All: 1

Review: 0

Click to change filter selection through MyNCBI.

1: J Invest Dermatol. 2000 May;114(5):1065-6. Links

A novel point mutation of the FALDH gene in a Japanese family with Sjögren-Larsson syndrome.

Aoki N, Suzuki H, Ito K, Ito M.

PMID: 10792573 [PubMed - indexed for MEDLINE]

Related articles

A novel 4 bp deletion mutation in the FALDH gene segregating in a Turkish family with Sjögren-Larsson syndrome.
J Invest Dermatol. 1999 May; 112(5):827-8.

[J Invest Dermatol. 1999]
A missense mutation in the FALDH gene identified in Sjögren-Larsson syndrome patients originating from the northern part of Sweden.
Hum Genet. 1997 Aug; 100(2):201-3.

[Hum Genet. 1997]
Novel ALDH3A2 heterozygous mutations in a Japanese family with Sjögren-Larsson syndrome.
J Invest Dermatol. 2006 Nov; 126(11):2545-7. Epub 2006 Jun 22.

[J Invest Dermatol. 2006]
ReviewSjögren-Larsson syndrome: molecular genetics and biochemical pathogenesis of fatty aldehyde dehydrogenase deficiency.
Mol Genet Metab. 2007 Jan; 90(1):1-9. Epub 2006 Sep 22.

[Mol Genet Metab. 2007]
ReviewSjögren-Larsson syndrome: diversity of mutations and polymorphisms in the fatty aldehyde dehydrogenase gene (ALDH3A2).
Hum Mutat. 2005 Jul; 26(1):1-10.

[Hum Mutat. 2005]
» See reviews... | » See all...

Recent Activity

Clear Turn Off Turn On

A novel point mutation of the FALDH gene in a Japanese family with Sjögren-Larsson syndrom...A novel point mutation of the FALDH gene in a Japanese family with Sjögren-Larsson syndrome.

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Display Show