Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

Nature Genetics

Volumn 17, Issue 2, 1997, Pages 171-178

  Simon, David B ^a   Bindra, Ranjit S ^a   Mansfield, Traci A ^a   Nelson Williams, Carol ^a   Mendonca, Erica ^b   Stone, Rosário ^b   Schurman, Scott ^c   Nayir, Ahmet ^d   Alpay, Harika ^d   Bakkaloglu, Aysin ^e   Rodriguez Soriano, Juan ^f   Morales, Jose M ^g   Sanjad, Sami A ^h   Mark Taylor, C ⁱ   Pilz, Daniela ^j   Brem, Andrew ^k   Trachtman, Howard ^l   Griswold, William ^m   Richard, George A ⁿ   John, Eunice ^o   Lifton, Richard P ^a   more..

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b HOSPITAL DE SANTA MARIA   (Portugal)

^c JOHNS HOPKINS ALL CHILDREN S HOSPITAL   (United States)

^d ISTANBUL UNIVERSITY   (Turkey)

^e HACETTEPE UNIVERSITY   (Turkey)

^f HOSPITAL DE CRUCES   (Spain)

^g HOSPITAL UNIVERSITARIO 12 DE OCTUBRE   (Spain)

^h KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTER   (Saudi Arabia)

ⁱ BIRMINGHAM CHILDREN S HOSPITAL   (United Kingdom)

^j UNIVERSITY HOSPITAL OF WALES   (United Kingdom)

^k RHODE ISLAND HOSPITAL   (United States)

^l ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^m RADY CHILDREN'S HOSPITAL   (United States)

ⁿ UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE   (United States)

^o UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

CHLORIDE CHANNEL;

ARTICLE; BARTTER SYNDROME; CALCIUM URINE LEVEL; CLINICAL FEATURE; GENE DELETION; HUMAN; HYPOKALEMIA; HYPOTENSION; PRIORITY JOURNAL; SALT LOSING NEPHRITIS;

BARTTER SYNDROME; BASE SEQUENCE; CHLORIDE CHANNELS; CHROMOSOMES, HUMAN, PAIR 1; CROSSING OVER, GENETIC; DNA PRIMERS; EXONS; FEMALE; HUMANS; INTRONS; LINKAGE (GENETICS); LOOP OF HENLE; MALE; MUTATION; PEDIGREE; PHENOTYPE; POLYMERASE CHAIN REACTION; SEQUENCE DELETION;

EID: 16944366243     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng1097-171     Document Type: Article

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