Mutations in the Hepatocyte Nuclear Factor-1β Gene Are Associated with Familial Hypoplastic Glomerulocystic Kidney Disease-Reference-Cited by-同舟云学术

Mutations in the Hepatocyte Nuclear Factor-1β Gene Are Associated with Familial Hypoplastic Glomerulocystic Kidney Disease

Published:2001-01 Issue:1 Volume:68 Page:219-224
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Bingham Coralie,Bulman Michael P.,Ellard Sian,Allen Lisa I.S.,Lipkin Graham W.,Hoff William G. van't,Woolf Adrian S.,Rizzoni Gianfranco,Novelli Giuseppe,Nicholls Anthony J.,Hattersley Andrew T.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference20 articles.

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2. Mutations in hepatocyte nuclear factor 1b are not a common cause of maturity-onset diabetes of the young in the U.K;Beards;Diabetes,1998

3. Glomerulocystic kidney disease—nosological considerations;Bernstein;Pediatr Nephrol,1993

4. Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1b;Bingham;Kidney Int,2000

5. Oral-facial-digital syndrome type 1 is another dominant polycystic kidney disease: clinical, radiological and histopathological features of a new kindred;Feather;Nephrol Dial Transplant,1997

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