Lack of sequence variations in the C4b-BP β-chain in patients with type III protein S deficiency bearing the Ser 460 to Pro mutation: Description of two new intragenic isomorphisms in the C4b-BP β-chain gene (C4BPB)

British Journal of Haematology

Volumn 101, Issue 1, 1998, Pages 10-15

  Morbœef, Olivier ^a   Aiach, Martine ^a   Gandrille, Sophie ^a  

^a INSERM   (France)

Author keywords

C4b BP chain gene; Coagulation inhibitors; Mutations; Protein S; PS type III deficiency phenotype

Indexed keywords

PROLINE; SERINE;

ALTERNATIVE RNA SPLICING; AMINO ACID SUBSTITUTION; ARTICLE; ENZYME DEFICIENCY; GENE LOCATION; GENE MUTATION; GENETIC POLYMORPHISM; HAPLOTYPE; HUMAN; INTRON; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN S DEFICIENCY;

EID: 0031958731     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.1998.00646.x     Document Type: Article

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