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Volumn 54, Issue 3, 2001, Pages 321-327
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Analysis of Btk mutations in patients with X-linked agammaglobulinaemia (XLA) and determination of carrier status in normal female relatives: A nationwide study of Btk deficiency in Greece
h
NONE
(Greece)
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Author keywords
[No Author keywords available]
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Indexed keywords
BRUTON TYROSINE KINASE;
COMPLEMENTARY DNA;
GENOMIC DNA;
PRIMER DNA;
PROTEIN TYROSINE KINASE;
UNCLASSIFIED DRUG;
ADOLESCENT;
ADULT;
ARTICLE;
ASSAY;
CHILD;
CLINICAL ARTICLE;
CODON;
CONTROLLED STUDY;
DIAGNOSTIC ACCURACY;
ENZYME DEFICIENCY;
EXON;
FEMALE;
FRAMESHIFT MUTATION;
GENE AMPLIFICATION;
GENE MUTATION;
GENE STRUCTURE;
GENETIC ASSOCIATION;
GREECE;
HETEROZYGOTE DETECTION;
HUMAN;
MALE;
MISSENSE MUTATION;
MOLECULAR GENETICS;
NON ISOTROPIC RIBONUCLEASE CLEAVAGE ASSAY;
NONSENSE MUTATION;
NUCLEIC ACID BASE SUBSTITUTION;
PHENOTYPE;
POLYMERASE CHAIN REACTION;
PRIORITY JOURNAL;
RELATIVE;
RELIABILITY;
SEQUENCE ANALYSIS;
X LINKED AGAMMAGLOBULINEMIA;
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EID: 0035720573
PISSN: 03009475
EISSN: None
Source Type: Journal
DOI: 10.1046/j.1365-3083.2001.00967.x Document Type: Article |
Times cited : (18)
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References (44)
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