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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1994 | 1 |
2000 | 1 |
2013 | 2 |
2024 | 0 |
PubMed (cited) for id: 600463
4 results
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ALDH1A3 loss of function causes bilateral anophthalmia/microphthalmia and hypoplasia of the optic nerve and optic chiasm.
Hum Mol Genet. 2013 Aug 15;22(16):3250-8. doi: 10.1093/hmg/ddt179. Epub 2013 Apr 15.
Hum Mol Genet. 2013.
PMID: 23591992
Free PMC article.
ALDH1A3 mutations cause recessive anophthalmia and microphthalmia.
Fares-Taie L, Gerber S, Chassaing N, Clayton-Smith J, Hanein S, Silva E, Serey M, Serre V, Gérard X, Baumann C, Plessis G, Demeer B, Brétillon L, Bole C, Nitschke P, Munnich A, Lyonnet S, Calvas P, Kaplan J, Ragge N, Rozet JM.
Fares-Taie L, et al.
Am J Hum Genet. 2013 Feb 7;92(2):265-70. doi: 10.1016/j.ajhg.2012.12.003. Epub 2013 Jan 9.
Am J Hum Genet. 2013.
PMID: 23312594
Free PMC article.
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Aldehyde dehydrogenase 6, a cytosolic retinaldehyde dehydrogenase prominently expressed in sensory neuroepithelia during development.
Grün F, Hirose Y, Kawauchi S, Ogura T, Umesono K.
Grün F, et al.
J Biol Chem. 2000 Dec 29;275(52):41210-8. doi: 10.1074/jbc.M007376200.
J Biol Chem. 2000.
PMID: 11013254
Free article.
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Molecular cloning, genomic organization, and chromosomal localization of an additional human aldehyde dehydrogenase gene, ALDH6.
Hsu LC, Chang WC, Hiraoka L, Hsieh CL.
Hsu LC, et al.
Genomics. 1994 Nov 15;24(2):333-41. doi: 10.1006/geno.1994.1624.
Genomics. 1994.
PMID: 7698756
Free article.
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