Erratum: A new and a reclassified ICF patient without mutations in DNMT3B and its interacting proteins SUMO-1 and UBC9 (American Journal of Medical Genetics (July 1, 2005) 136A (31-37) DOI 10.1002/ajmg.a.30767);A new and a reclassified ICF patient without mutations in DNMT3B and its interacting proteins SUMO-1 and UBC9

American Journal of Medical Genetics

Volumn 136 A, Issue 1, 2005, Pages 31-37

  Kloeckener Gruissem, Barbara ^a,d   Betts, David R ^b   Zankl, Andreas ^a,c   Berger, Wolfgang ^a   Güngör, Tayfun ^b  

^a UNIVERSITY OF ZURICH   (Switzerland)

^b UNIVERSITY CHILDREN S HOSPITAL   (Switzerland)

^c LAUSANNE UNIVERSITY HOSPITAL   (Switzerland)

^d Institute of Medical Genetics   (Switzerland)

Author keywords

DNA hypomethylation; ICF syndrome; Methyltransferase DNMT3B; SUMO 1; UBC9

Indexed keywords

METHYLTRANSFERASE; PROTEIN UBC9; SATELLITE DNA; SUMO 1 PROTEIN;

ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CENTROMERE; CHROMOSOMAL INSTABILITY; CHROMOSOME 1; CHROMOSOME 16; CLINICAL FEATURE; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; CYTOGENETICS; DNA METHYLATION; DNMT3B GENE; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC CODE; HUMAN; HUMAN CELL; ICF SYNDROME; IHRDIP SYNDROME; IMMUNODEFICIENCY CENTROMERIC INSTABILITY FACIAL ANOMALIES SYNDROME; ISCHIADIC HYPOPLASIA RENAL DYSGENESIS IMMUNODEFICIENCY AND POLYDACTYLY SYNDROME; MALE; MULTIPLE MALFORMATION SYNDROME; NUCLEOTIDE SEQUENCE; PATIENT CODING; PRESCHOOL CHILD; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN DNA INTERACTION; RNA SPLICING;

EID: 21644474867     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30930     Document Type: Erratum

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