A deletion/insertion leading to the generation of a direct repeat as a result of slipped mispairing and intragenic recombination in the factor VIII gene

Human Genetics

Volumn 104, Issue 5, 1999, Pages 435-437

  Tavassoli, Kamiab ^a   Eigel, Antonin ^a   Horst, Jürgen ^a  

^a UNIVERSITY OF MÜNSTER   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 8;

ARTICLE; CASE REPORT; EXON; GENE DELETION; GENE DUPLICATION; GENE INSERTION; GENETIC RECOMBINATION; HEMOPHILIA A; HUMAN; INTRON; PRIORITY JOURNAL;

BASE PAIRING; BASE SEQUENCE; DEOXYRIBONUCLEASES, TYPE II SITE-SPECIFIC; DNA; DNA TRANSPOSABLE ELEMENTS; EXONS; FACTOR VIII; HEMOPHILIA A; HUMANS; INTRONS; LYMPHOCYTES; NUCLEIC ACID CONFORMATION; POLYMERASE CHAIN REACTION; RECOMBINATION, GENETIC; REPETITIVE SEQUENCES, NUCLEIC ACID; RESTRICTION MAPPING; SEQUENCE DELETION;

EID: 0032995699     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050981     Document Type: Article

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