Novel NPR1 polymorphic variants and its exclusion as a candidate gene for medullary cystic kidney disease (ADMCKD) type 1

Molecular and Cellular Probes

Volumn 15, Issue 6, 2001, Pages 357-361

  Koptides, Michael ^a   Mean, Richard ^a   Stavrou, Christoforos ^b   Pierides, Alkis ^c   Demetriou, Kyproula ^c   Nakayama, Tomohiro ^d   Hildebrandt, Friedhelm ^e   Fuchshuber, Arno ^e   Deltas, C Constantinou ^a  

^a CYPRUS INSTITUTE OF NEUROLOGY AND GENETICS   (Cyprus)

^b Pafos General Hospital   (Cyprus)

^c NICOSIA GENERAL HOSPITAL   (Cyprus)

^d NIHON UNIVERSITY   (Japan)

^e UNIVERSITY OF FREIBURG   (Germany)

Author keywords

Cystic kidneys; Hypertension; Hypotension; MCKD1; NPR1; Polymorphisms

Indexed keywords

ARGININE; ATRIAL NATRIURETIC FACTOR RECEPTOR; ATRIAL NATRIURETIC FACTOR RECEPTOR 1; DNA; GLUTAMINE; UNCLASSIFIED DRUG;

3' UNTRANSLATED REGION; 5' UNTRANSLATED REGION; ALLELE; AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BLOOD PRESSURE REGULATION; CHROMOSOME 1Q; DNA POLYMORPHISM; DNA SCREENING; GENE DELETION; GENE FUNCTION; GENE INSERTION; GENE LOCUS; GENE MAPPING; GENE SEQUENCE; HUMAN; HUMAN CELL; KIDNEY FAILURE; MAJOR CLINICAL STUDY; MARKER GENE; MEDULLARY SPONGE KIDNEY; MUTATIONAL ANALYSIS; ONSET AGE; PRIORITY JOURNAL; SALT LOSING NEPHRITIS; SODIUM EXCRETION; STOP CODON;

INSERTION SEQUENCES;

EID: 0035722095     PISSN: 08908508     EISSN: None     Source Type: Journal    
DOI: 10.1006/mcpr.2001.0381     Document Type: Article

References (20)

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