METHOD AND PROBES FOR DETECTION OF ALPORT SYNDROME
摘要
<p>The present invention relates to a method for identifying an individual possessing a genetic defect associated with Alport syndrome which comprises analyzing the DNA of the individual to be tested by a method capable of detecting variation in a DNA sequence, and observing the presence or absence of a variation in the COL4A5 gene, in comparison with a normal COL4A5 gene.</p>
申请公布号
WO9119010(A1)
申请公布日期
1991.12.12
申请号
WO1991US04051
申请日期
1991.06.07
申请人
UNIVERSITY OF UTAH;TRYGGVASON, KARL;HOSTIKKA, SIRKKA, LIISA
