Three different premature stop codons lead to skipping of exon 7 in neurofibromatosis type I patients

Human mutation

Volumn 16, Issue 1, 2000, Pages 90-91

  Wimmer, Katharina ^a   Eckart, Markus ^a   Stadler, Peter F ^a   Rehder, Helga ^a   Fonatsch, Christa ^a  

^a UNIVERSITY OF VIENNA   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; COMPARATIVE STUDY; EXON; GENE DELETION; GENETICS; HUMAN; METHODOLOGY; MOLECULAR GENETICS; NEUROFIBROMATOSIS; NUCLEOTIDE SEQUENCE; STOP CODON;

BASE SEQUENCE; CODON, TERMINATOR; DNA MUTATIONAL ANALYSIS; EXONS; HUMANS; MOLECULAR SEQUENCE DATA; NEUROFIBROMATOSIS 1; SEQUENCE DELETION;

EID: 0034219209     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/1098-1004(200007)16:1<90::AID-HUMU20>3.0.CO;2-J     Document Type: Article

References (0)