Literature DB >> 12515373

Monogenic renal diseases: a clinical introduction.

Jean-Pierre Grünfeld1.   

Abstract

The clinical spectrum of monogenic renal diseases is wide ranging, from autosomal dominant polycystic kidney disease to very rare inherited disorders. The genes involved in most of these diseases have been identified. However some monogenic diseases are still not characterized clinically. The challenges of the future will be to understand phenotypic variability and the molecular mechanisms of disease, and to design pharmacological tools to stop or retard its progression. The post-gene era has begun and the field of research in monogenic disorders is wide open.

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Year:  2002        PMID: 12515373

Source DB:  PubMed          Journal:  J Nephrol        ISSN: 1121-8428            Impact factor:   3.902


  1 in total

1.  Splice-site mutations identified in PDE6A responsible for retinitis pigmentosa in consanguineous Pakistani families.

Authors:  Shahid Y Khan; Shahbaz Ali; Muhammad Asif Naeem; Shaheen N Khan; Tayyab Husnain; Nadeem H Butt; Zaheeruddin A Qazi; Javed Akram; Sheikh Riazuddin; Radha Ayyagari; J Fielding Hejtmancik; S Amer Riazuddin
Journal:  Mol Vis       Date:  2015-08-18       Impact factor: 2.367

  1 in total

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