LMX1B mutation with residual transcriptional activity as a cause of isolated glomerulopathy-Reference-Cited by-同舟云学术

LMX1B mutation with residual transcriptional activity as a cause of isolated glomerulopathy

Published:2013-09-15 Issue:1 Volume:29 Page:81-88
ISSN:1460-2385
Container-title:Nephrology Dialysis Transplantation
language:en
Short-container-title:

Author:

Isojima Tsuyoshi,Harita Yutaka,Furuyama Masayuki,Sugawara Noriko,Ishizuka Kiyonobu,Horita Shigeru,Kajiho Yuko,Miura Kenichiro,Igarashi Takashi,Hattori Motoshi,Kitanaka Sachiko

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ndt/article-pdf/29/1/81/17172979/gft359.pdf

Reference23 articles.

1. Hereditary onycho-osteodysplasia (nail-patella syndrome). A report of nine kindreds;Beals;J Bone Joint Surg Am,1969

2. Cosegregation of open-angle glaucoma and the nail-patella syndrome;Lichter;Am J Ophthalmol,1997

3. Nail patella syndrome: a review of the phenotype aided by developmental biology;Sweeney;J Med Genet,2003

4. Loss-of-function mutations in the LIM-homeodomain gene, LMX1B, in nail-patella syndrome;Vollrath;Hum Mol Genet,1998

5. Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome;Dreyer;Nat Genet,1998

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