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Year | Number of Results |
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2002 | 1 |
2006 | 1 |
2007 | 1 |
2014 | 1 |
2024 | 0 |
PubMed (cited) for id: 610202
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Identification of a novel missense mutation of MAF in a Japanese family with congenital cataract by whole exome sequencing: a clinical report and review of literature.
Am J Med Genet A. 2014 May;164A(5):1272-6. doi: 10.1002/ajmg.a.36433. Epub 2014 Mar 24.
Am J Med Genet A. 2014.
PMID: 24664492
Review.
Novel MAF mutation in a family with congenital cataract-microcornea syndrome.
Hansen L, Eiberg H, Rosenberg T.
Hansen L, et al.
Mol Vis. 2007 Oct 18;13:2019-22.
Mol Vis. 2007.
PMID: 17982426
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A novel mutation in the DNA-binding domain of MAF at 16q23.1 associated with autosomal dominant "cerulean cataract" in an Indian family.
Vanita V, Singh D, Robinson PN, Sperling K, Singh JR.
Vanita V, et al.
Am J Med Genet A. 2006 Mar 15;140(6):558-66. doi: 10.1002/ajmg.a.31126.
Am J Med Genet A. 2006.
PMID: 16470690
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Domain disruption and mutation of the bZIP transcription factor, MAF, associated with cataract, ocular anterior segment dysgenesis and coloboma.
Jamieson RV, Perveen R, Kerr B, Carette M, Yardley J, Heon E, Wirth MG, van Heyningen V, Donnai D, Munier F, Black GC.
Jamieson RV, et al.
Hum Mol Genet. 2002 Jan 1;11(1):33-42. doi: 10.1093/hmg/11.1.33.
Hum Mol Genet. 2002.
PMID: 11772997
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