A founder mutation in LEPRE1 carried by 1.5% of West Africans and 0.4% of African Americans causes lethal recessive osteogenesis imperfecta.
第一作者:
Wayne A,Cabral
第一单位:
Bone and Extracellular Matrix Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA.
作者:
医学主题词
队列研究(Cohort Studies);DNA(DNA);建立者效应(Founder Effect);加纳(Ghana);杂合子(Heterozygote);人类(Humans);婴儿, 新生(Infant, Newborn);连锁不平衡(Linkage Disequilibrium);膜糖蛋白类(Membrane Glycoproteins);突变(Mutation);尼日利亚(Nigeria);北美洲(North America);成骨不全(Osteogenesis Imperfecta);蛋白聚糖类(Proteoglycans)
DOI
10.1038/gim.2011.44
PMID
22281939
发布时间
2025-05-29
- 浏览19
Genetics in medicine
543-51页
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