McLeod syndrome resulting from a novel XK mutation

British Journal of Haematology

Volumn 122, Issue 4, 2003, Pages 682-685

  Singleton, Belinda K ^a   Green, Carole A ^a   Renaud, Susanne ^b   Fuhr, Peter ^b   Poole, Joyce ^a   Daniels, Geoff L ^a  

^a NHS BLOOD AND TRANSPLANT   (United Kingdom)

^b UNIVERSITY HOSPITAL BASEL   (Switzerland)

Author keywords

Kell antigens; Kx protein; McLeod Syndrome; MLS; XK gene

Indexed keywords

ALANINE AMINOTRANSFERASE; ANTIGEN; ASPARTATE AMINOTRANSFERASE; CREATINE KINASE; GENOMIC DNA; KX ANTIGEN; LACTATE DEHYDROGENASE; LIVER ENZYME; UNCLASSIFIED DRUG;

ACANTHOCYTOSIS; ADULT; AGGRESSION; ALLELE; ANTIGEN EXPRESSION; ARTICLE; BLOOD DISEASE; BLOOD GROUP; BLOOD GROUP KELL SYSTEM; BLOOD SMEAR; CARDIOMYOPATHY; CASE REPORT; CELL ASSAY; CHOREA; CLINICAL FEATURE; DEMENTIA; DISEASE ASSOCIATION; DISEASE COURSE; ELECTROMYOGRAPHY; ELECTRONEUROGRAPHY; ENZYME BLOOD LEVEL; ERYTHROCYTE; EXON; FLOW CYTOMETRY; GENE DELETION; GENE LOCATION; GENE MUTATION; HEMIZYGOSITY; HETEROZYGOTE; HUMAN; HYPERTRANSLUCENT LUNG; MALE; MUSCLE DISEASE; NEUROLOGIC DISEASE; NUCLEOTIDE SEQUENCE; ONSET AGE; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SERODIAGNOSIS; SYMPTOM; X CHROMOSOME LINKED DISORDER;

AMINO ACID TRANSPORT SYSTEMS, NEUTRAL; BASE SEQUENCE; FEMALE; GENE DELETION; GENETIC DISEASES, X-LINKED; HEMATOLOGIC DISEASES; HUMANS; KELL BLOOD-GROUP SYSTEM; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; NEUROMUSCULAR DISEASES; SYNDROME;

EID: 0042662876     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.2003.04474.x     Document Type: Article

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