Peters D J, Spruit L, Saris J J, Ravine D, Sandkuijl L A, Fossdal R, Boersma J, van Eijk R, Nørby S, Constantinou-Deltas C D
Department of Human Genetics, Leiden University, Sylvius Laboratories, The Netherlands.
Nat Genet. 1993 Dec;5(4):359-62. doi: 10.1038/ng1293-359.
Autosomal dominant polycystic kidney disease (ADPKD) is a genetically heterogeneous disorder. A gene defect located on the short arm of chromosome 16 is responsible for the disease in roughly 86% of affected European families. Using highly polymorphic microsatellite DNA markers, we have assigned a second gene for ADPKD to chromosome 4. In eight families with clear evidence against linkage to chromosome 16 markers, linkage analysis with the markers D4S231 and D4S423, demonstrated a multipoint lod score of 22.42.
常染色体显性多囊肾病(ADPKD)是一种基因异质性疾病。位于16号染色体短臂上的一个基因缺陷导致了大约86%的欧洲患病家庭出现这种疾病。我们利用高度多态的微卫星DNA标记,将ADPKD的第二个基因定位于4号染色体。在八个明确显示与16号染色体标记无连锁关系的家庭中,用标记D4S231和D4S423进行连锁分析,得到的多点对数优势分数为22.42。