Apparently dominant transmission of a recessive disease: Deficiency of factor vii in iranian jews

Annali Italiani di Medicina Interna

Volumn 15, Issue 4, 2000, Pages 263-266

  Tagliabue, L ^a   Duca, F ^a   Peyvandi, F ^a  

^a UNIVERSITY OF MILAN   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BLOOD CLOTTING FACTOR 7 DEFICIENCY; CASE REPORT; CLINICAL FEATURE; DISEASE TRANSMISSION; DNA DETERMINATION; FEMALE; HUMAN; IRAN; MISSENSE MUTATION; PEDIGREE;

ADULT; CHILD; DNA MUTATIONAL ANALYSIS; FACTOR VII DEFICIENCY; FEMALE; GENES, RECESSIVE; HUMANS; IRAN; JEWS; MALE; MUTATION, MISSENSE; PEDIGREE; PHENOTYPE;

EID: 0034491374     PISSN: 03939340     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

1. Purification and properties of human coagulation factor VII
2. q34. Expression of factor VII through chromosome 8
3. Clinical manifestations in 28 Italian and Iranian patients with severe factor VII deficiency
4. Rare coagulation disorders
5. Ala244Val is a common, probably ancient mutation causing factor VII deficiency in Moroccan and Iranian Jews
6. Nucleotide sequence of the gene coding for human factor VII, a vitamin K-dependent protein participating in blood coagulation