Molecular and clinical studies of Dent's disease in Japan: Biochemical examination and renal ultrasonography do not predict carrier state

Clinical Nephrology

Volumn 61, Issue 4, 2004, Pages 231-237

  Matsuyama, T ^a   Awazu, M ^b   Oikawa, T ^c   Inatomi, J ^d   Sekine, T ^d   Igarashi, T ^d  

^a UNIVERSITY OF TOKYO   (Japan)

^b KEIO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c JIKEI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^d UNIVERSITY OF TOKYO   (Japan)

Author keywords

Dent's disease; Gene mutation; Nephrocalcinosis; Proteinuria; 2 microglobulin

Indexed keywords

ALPHA 1 MICROGLOBULIN; BETA 2 MICROGLOBULIN; CALCIUM; CELL DNA; CREATININE; DNA BASE; GENE PRODUCT; NUCLEOTIDE; PRIMER DNA; RETINOL BINDING PROTEIN;

ADULT; ARTICLE; BETA 2 MICROGLOBULIN URINE LEVEL; BIOCHEMISTRY; CALCIUM URINE LEVEL; CHILD; CLINICAL ARTICLE; CLINICAL EXAMINATION; CLINICAL STUDY; CONTROLLED STUDY; CREATININE URINE LEVEL; DENT DISEASE; DNA SEQUENCE; ECHOGRAPHY; EXON; FAMILY; FEMALE; FREQUENCY ANALYSIS; GENE AMPLIFICATION; GENE INSERTION SEQUENCE; GENE MUTATION; GENE STRUCTURE; GENETIC CODE; HETEROZYGOTE DETECTION; HUMAN; HYPERCALCIURIA; HYPOPHOSPHATEMIA; INTRON; JAPAN; KIDNEY CALCIFICATION; KIDNEY TUBULE DISORDER; LEUKOCYTE; MALE; MISSENSE MUTATION; MOLECULAR WEIGHT; MOTHER; NEPHROLITHIASIS; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PREDICTION; PROTEIN URINE LEVEL; PROTEINURIA; URINE OSMOLALITY; X CHROMOSOME LINKED DISORDER;

EID: 1842689705     PISSN: 03010430     EISSN: None     Source Type: Journal    
DOI: 10.5414/CNP61231     Document Type: Article

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