ABCA12 mutations in patients with autosomal recessive congenital ichthyosis: evidence of a founder effect in the Spanish population and phenotype-genotype implications.
作者:
主题词
ATP结合匣式转运子(ATP-Binding Cassette Transporters);密码子, 无义(Codon, Nonsense);DNA突变分析(DNA Mutational Analysis);女(雌)性(Female);建立者效应(Founder Effect);遗传关联研究(Genetic Association Studies);疾病遗传易感性(Genetic Predisposition to Disease);单倍型(Haplotypes);遗传(Heredity);人类(Humans);鳞癣样红皮病, 先天性(Ichthyosiform Erythroderma, Congenital);鳞癣, 板层状(Ichthyosis, Lamellar);男(雄)性(Male);突变, 误义(Mutation, Missense);表型(Phenotype);西班牙(Spain)
DOI
10.1016/j.jdermsci.2018.05.012
PMID
29887490
发布时间
2019-06-17
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