Erratum: Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia (Human Genetics DOI: 10.1007/s00439-009-0766-y);Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia

Human Genetics

Volumn 127, Issue 2, 2010, Pages 231-241

  Connell, Fiona ^a   Kalidas, Kamini ^a   Ostergaard, Pia ^a   Brice, Glen ^a   Homfray, Tessa ^a   Roberts, Lesley ^b   Bunyan, David J ^c   Mitton, Sally ^a   Mansour, Sahar ^a   Mortimer, Peter ^a   Jeffery, Steve ^a  

^a ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

^b KING S COLLEGE HOSPITAL   (United Kingdom)

^c SALISBURY DISTRICT HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALBUMIN; BINDING PROTEIN; COLLAGEN AND CALCIUM BINDING EGF DOMAIN 1 PROTEIN; CYSTEINE; OCTREOTIDE; SERINE; SPIRONOLACTONE; UNCLASSIFIED DRUG; CALCIUM BINDING PROTEIN; CCBE1 PROTEIN, HUMAN; TUMOR SUPPRESSOR PROTEIN;

AMINO ACID SUBSTITUTION; ARTICLE; ASCITES; BRAIN VENTRICLE PERITONEUM SHUNT; CASE REPORT; CHILD; CHROMOSOME 18; DIET THERAPY; FEMALE; FETUS HYDROPS; GENE MUTATION; GENE SEQUENCE; GENERALIZED LYMPHATIC DYSPLASIA; GENETIC LINKAGE; HOMOZYGOSITY; HUMAN; INFANT; INTESTINE LYMPHANGIECTASIA; LYMPHATIC SYSTEM DISEASE; LYMPHEDEMA; MALE; PERIPHERAL EDEMA; PRESCHOOL CHILD; PRIORITY JOURNAL; RECESSIVE INHERITANCE; SINGLE NUCLEOTIDE POLYMORPHISM; SPONTANEOUS ABORTION; CHROMOSOME MAP; FAMILY HEALTH; FATALITY; FETUS DEATH; GENETIC PREDISPOSITION; GENETICS; GENOTYPE; METHODOLOGY; MUTATION; NUCLEOTIDE SEQUENCE; PATHOLOGY; PEDIGREE; RECESSIVE GENE;

DANIO RERIO;

BASE SEQUENCE; CALCIUM-BINDING PROTEINS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 18; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; FATAL OUTCOME; FEMALE; FETAL DEATH; GENES, RECESSIVE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; INFANT; LINKAGE (GENETICS); LYMPHEDEMA; MALE; MUTATION; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE; TUMOR SUPPRESSOR PROTEINS;

EID: 76249099579     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/s00439-009-0772-0     Document Type: Erratum

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