Medullary cystic kidney disease type 1: Mutational analysis in 37 genes based on haplotype sharing

Human Genetics

Volumn 119, Issue 6, 2006, Pages 649-658

  Wolf, Matthias T F ^a,e,f   Mucha, Bettina E ^a   Hennies, Hans C ^b   Attanasio, Massimo ^a   Panther, Franziska ^a   Zalewski, Isabella ^a   Karle, Stephanie M ^c   Otto, Edgar A ^a   Deltas, C Constantinou ^d   Fuchshuber, Arno ^c   Hildebrandt, Friedhelm ^a,g  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^b MAX DELBRÜCK CENTER FOR MOLECULAR MEDICINE   (Germany)

^c UNIVERSITY OF FREIBURG   (Germany)

^d CYPRUS INSTITUTE OF NEUROLOGY AND GENETICS   (Cyprus)

^e UNIVERSITY HOSPITAL OF COLOGNE   (Germany)

^f UNIVERSITY OF COLOGNE   (Germany)

^g UNIVERSITY OF MICHIGAN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BELGIUM; BLOOD SAMPLING; CHILD; CONTROLLED STUDY; EXON; FEMALE; GENE FUNCTION; GENE MUTATION; GENE SEGREGATION; GENE SEQUENCE; GENETIC RECOMBINATION; GENETIC SCREENING; GENETIC VARIABILITY; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; MEDULLARY SPONGE KIDNEY; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RNA SPLICING; SEQUENCE ANALYSIS;

CHROMOSOME MAPPING; DNA MUTATIONAL ANALYSIS; HAPLOTYPES; HUMANS; MEDULLARY SPONGE KIDNEY; MICROSATELLITE REPEATS;

EID: 33744475145     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-006-0176-3     Document Type: Article

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