Erratum: Familial hypercatabolic hypoproteinemia caused by deficiency of the neonatal Fc receptor, FcRn, due to a mutant β2-microglobulin gene (Proceedings of the National Academy of Sciences of the United States of America (March 28, 2006) 13, 103 (5084-5089) DOI: 10.1073/pnas.0600548103);Familial hypercatabolic hypoproteinemia caused by deficiency of the neonatal Fc receptor, FcRn, due to a mutant β2-microglobulin gene

Proceedings of the National Academy of Sciences of the United States of America

Volumn 103, Issue 13, 2006, Pages 5084-5089

  Wani, Manzoor A ^a   Haynes, Lynn D ^b   Kim, Jonghan ^a   Bronson, C L ^a   Chaudhury, Chaity ^a   Mohanty, Sudhasri ^a   Waldmann, Thomas A ^c   Robinson, John M ^a   Anderson, Clark L ^a,d  

^a OHIO STATE UNIVERSITY   (United States)

^b UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

^c NATIONAL CANCER INSTITUTE   (United States)

^d 415 HLRI ^*  (United States)

Author keywords

Albumin; Hypoalbuminemia; Hypogammaglobulinemia; IgG; MHC class I

Indexed keywords

ALANINE; ALBUMIN; BETA 2 MICROGLOBULIN; COMPLEMENTARY DNA; FC RECEPTOR; HETERODIMER; IMMUNOGLOBULIN G; LIGAND; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 1; PROLINE; PROTEIN FCRN; UNCLASSIFIED DRUG;

AMINO ACID SUBSTITUTION; ANALBUMINEMIA; ARTICLE; CATABOLISM; CELL CULTURE; CONSANGUINEOUS MARRIAGE; CONTROLLED STUDY; FAMILIAL DISEASE; FAMILIAL HYPERCATABOLIC HYPOPROTEINEMIA; GENE MUTATION; GENE SEQUENCE; GENETIC TRANSFECTION; HUMAN; HUMAN CELL; HYPOPROTEINEMIA; IMMUNOGLOBULIN BLOOD LEVEL; IMMUNOGLOBULIN DEFICIENCY; LIGAND BINDING; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN DEGRADATION; SERUM; SIBLING; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 33645531322     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.0604332103     Document Type: Erratum

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