Literature DB >> 11733635

Late onset of renal disease in nephronophthisis with features of Joubert syndrome type B.

T Apostolou1, N Nikolopoulou, M Theodoridis, V Koumoustiotis, E Pavlopoulou, D Chondros, A Billis.   

Abstract

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Year:  2001        PMID： 11733635     DOI： 10.1093/ndt/16.12.2412

Source DB:  PubMed          Journal:  Nephrol Dial Transplant        ISSN： 0931-0509            Impact factor:   5.992


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  3 in total

1.  The NPHP1 gene deletion associated with juvenile nephronophthisis is present in a subset of individuals with Joubert syndrome.

Authors:  Melissa A Parisi; Craig L Bennett; Melissa L Eckert; William B Dobyns; Joseph G Gleeson; Dennis W W Shaw; Ruth McDonald; Allison Eddy; Phillip F Chance; Ian A Glass
Journal:  Am J Hum Genet       Date:  2004-05-11       Impact factor: 11.025

Review 2.  Review of Ocular Manifestations of Joubert Syndrome.

Authors:  Stephanie F Wang; Tia J Kowal; Ke Ning; Euna B Koo; Albert Y Wu; Vinit B Mahajan; Yang Sun
Journal:  Genes (Basel)       Date:  2018-12-04       Impact factor: 4.096

3.  DDA: A Novel Network-Based Scoring Method to Identify Disease-Disease Associations.

Authors:  Apichat Suratanee; Kitiporn Plaimas
Journal:  Bioinform Biol Insights       Date:  2015-12-08
  3 in total

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