Polycystic kidney disease. 1: Identification and analysis of the primary defect.

Harris, P C; Ward, C J; Peral, B; Hughes, J

Harris, P C; Ward, C J; Peral, B; Hughes, J.

J Am Soc Nephrol ; 6(4): 1125-33, 1995 Oct.

Article in En | MEDLINE | ID: mdl-8589278

Subject(s)

Chromosome Mapping; Polycystic Kidney, Autosomal Dominant/genetics; Polycystic Kidney, Autosomal Dominant/metabolism; Cloning, Molecular; Genes; Humans; Mutation; Proteins/genetics; Proteins/metabolism; Sequence Homology, Amino Acid; TRPP Cation Channels; Transcription, Genetic; Translocation, Genetic

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Collection: 01-internacional Database: MEDLINE Main subject: Chromosome Mapping / Polycystic Kidney, Autosomal Dominant Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: J Am Soc Nephrol Journal subject: NEFROLOGIA Year: 1995 Type: Article

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