Molecular diagnostics in autosomal dominant polycystic kidney disease: Utility and limitations

Clinical Journal of the American Society of Nephrology

Volumn 3, Issue 1, 2008, Pages 146-152

  Zhao, Xiao ^a   Paterson, Andrew D ^b   Zahirieh, Alireza ^a   He, Ning ^a   Wang, Kairong ^a   Pei, York ^a  

^a UNIVERSITY HEALTH NETWORK   (Canada)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

POLYCYSTIC KIDNEY DISEASE 1 PROTEIN; POLYCYSTIC KIDNEY DISEASE 2 PROTEIN; POLYCYSTIN; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; AGED; ARTICLE; CLINICAL TRIAL; FAMILY HEALTH; FEMALE; GENETIC LINKAGE; GENETIC SCREENING; GENETICS; HAPLOTYPE; HUMAN; KIDNEY POLYCYSTIC DISEASE; MALE; METHODOLOGY; MIDDLE AGED; NUCLEOTIDE SEQUENCE; PEDIGREE; STANDARD; VALIDATION STUDY;

ADOLESCENT; ADULT; AGED; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; FEMALE; GENETIC SCREENING; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); MALE; MIDDLE AGED; PEDIGREE; POLYCYSTIC KIDNEY, AUTOSOMAL DOMINANT; TRPP CATION CHANNELS;

EID: 38749112619     PISSN: 15559041     EISSN: 1555905X     Source Type: Journal    
DOI: 10.2215/CJN.03430807     Document Type: Article

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