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F13A 分配的确认以及关于 F13A - HLA - GLO 的序列信息。

Confirmation of F13A assignment and sequence information concerning F13A-HLA-GLO.

作者信息

Eiberg H, Nielsen L S, Mohr J

出版信息

Clin Genet. 1984 Nov;26(5):385-8. doi: 10.1111/j.1399-0004.1984.tb01077.x.

DOI:10.1111/j.1399-0004.1984.tb01077.x
PMID:6149828
Abstract

The polymorphism of the blood clotting factor F13A was examined in some of our Danish material of normal families. A total of four alleles were recognized, with allele frequencies as follows: F13A *1 = 0.817, F13A *2 = 0.177, F13A *4 = 0.003 and a new allele F13A *5 = 0.003. The distribution of unrelated individuals did not deviate significantly from the Hardy-Weinberg expectation. Linkage of F13A with HLA was confirmed (z = 5.18, theta = 0.17 in males and z = 0.14, theta = 0.37 in females). The sequence of the three systems F13A, HLA and GLO was found to be F13A-HLA-GLO as judged from two families each with a recombinant within the HLA system in males.

摘要

我们在一些丹麦正常家庭材料中检测了凝血因子F13A的多态性。共识别出四个等位基因,其等位基因频率如下:F13A *1 = 0.817,F13A *2 = 0.177,F13A *4 = 0.003以及一个新的等位基因F13A *5 = 0.003。无关个体的分布与哈迪-温伯格预期无显著偏差。证实了F13A与HLA的连锁关系(男性中z = 5.18,θ = 0.17;女性中z = 0.14,θ = 0.37)。从两个男性家庭中各有一个在HLA系统内发生重组的家庭判断,F13A、HLA和GLO这三个系统的顺序为F13A - HLA - GLO。

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Confirmation of F13A assignment and sequence information concerning F13A-HLA-GLO.F13A 分配的确认以及关于 F13A - HLA - GLO 的序列信息。
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引用本文的文献

1
Polymorphism of the A subunit of coagulation factor XIII: evidence for subtypes of the FXIIIA*1 and FXIIIA*2 alleles.凝血因子 XIII A 亚基的多态性:FXIIIA*1 和 FXIIIA*2 等位基因亚型的证据。
Am J Hum Genet. 1988 Aug;43(2):170-4.
2
Analysis for linkage between F13A and three chromosome 6 marker loci: evidence for 6pter:F13A:HLA:GLO1:cen gene order.F13A与三个6号染色体标记位点之间的连锁分析:6pter:F13A:HLA:GLO1:cen基因顺序的证据。
Hum Genet. 1988 Jul;79(3):228-30. doi: 10.1007/BF00366241.
3
Extensive DNA polymorphism at the factor XIIIa (F13A) locus and linkage to HLA.
Am J Hum Genet. 1988 Jun;42(6):877-83.
4
Haplotypes of the coagulation factor XIII A subunit locus in normal and deficient subjects.正常和缺乏凝血因子XIII A亚基位点的单倍型
Am J Hum Genet. 1988 May;42(5):712-7.
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Spinocerebellar ataxia: multipoint linkage analysis of genes associated with the disease locus.脊髓小脑共济失调:与疾病位点相关基因的多点连锁分析
Hum Genet. 1991 Aug;87(4):405-8. doi: 10.1007/BF00197157.