Carbonic anhydrase II (CA II) deficiency in Maghrebian patients: Evidence for founder effect and genomic recombination at the CA II locus

Human Genetics

Volumn 99, Issue 5, 1997, Pages 634-637

  Fathallah, Dahmani M ^a   Bejaoui, Mohamed ^b   Lepaslier, Denis ^c   Chater, Khelifa ^d   Sly, William S ^e   Dellagi, Koussay ^a  

^a PASTEUR INSTITUTE OF TUNIS   (Tunisia)

^b CHARLES NICOLLE HOSPITAL   (Tunisia)

^c FONDATION JEAN DAUSSET CEPH   (France)

^d UNIVERSITY OF TUNIS   (Tunisia)

^e SAINT LOUIS UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARBONATE DEHYDRATASE II;

ALBERS SCHOENBERG DISEASE; ARAB; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; ENZYME DEFICIENCY; ETHNIC GROUP; FAMILY STUDY; FEMALE; FOUNDER EFFECT; GENE MUTATION; GENETIC RECOMBINATION; HUMAN; HUMAN CELL; KIDNEY TUBULE ACIDOSIS; MALE; MENTAL DEFICIENCY; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SEQUENCE TAGGED SITE;

EID: 0030896802     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050419     Document Type: Article

References (19)

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