Familial transient erythroblastopenia of childhood is associated with the chromosome 19q13.2 region but not caused by mutations in coding sequences of the ribosomal protein S19 (RPS19) gene

British Journal of Haematology

Volumn 119, Issue 1, 2002, Pages 261-264

  Gustavsson, Peter ^a   Klar, Joakim ^a   Matsson, Hans ^a   Forestier, Erik ^b   Henter, Jan Inge ^c   Rao, Sreedhar ^d   Seip, Martin ^e   Skeppner, Gunnar ^f   Dahl, Niklas ^a  

^a UPPSALA UNIVERSITY HOSPITAL   (Sweden)

^b UMEÅ UNIVERSITY   (Sweden)

^c KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^d SUNY Downstate Medical Center   (United States)

^e OSLO UNIVERSITY HOSPITAL   (Norway)

^f ÖREBRO UNIVERSITY HOSPITAL   (Sweden)

Author keywords

Chromosome 19q13.2; Familial transient erythroblastopenia of childhood (TEC); Linkage analysis; Mutation detection; RPS19 gene

Indexed keywords

PROTEIN S19; RIBOSOME PROTEIN; UNCLASSIFIED DRUG;

ALLELISM; ARTICLE; CHILD; CHROMOSOME 19Q; CLINICAL ARTICLE; CODING; CONTROLLED STUDY; DISEASE ASSOCIATION; ERYTHROBLASTOPENIA; EXON; FAMILIAL DISEASE; GENE LOCUS; GENE MUTATION; GENE STRUCTURE; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC CODE; HUMAN; LINKAGE ANALYSIS; MARKER GENE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SIBLING;

ADULT; CHILD; CHROMOSOMES, HUMAN, PAIR 19; ERYTHROBLASTS; GENOTYPE; HEMATOLOGIC DISEASES; HUMANS; LINKAGE (GENETICS); MUTATION; PEDIGREE; RIBOSOMAL PROTEINS; SEQUENCE ANALYSIS;

EID: 0036398432     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.2002.03776.x     Document Type: Article

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