Alternative splicing in the fragile X gene FMR1

The FMR1 gene, associated with fragile X syndrome, has recently been cloned and the sequence of partial cDNA clones is known. We have determined additional cDNA sequences both at the 5' and 3' end. We have characterized the expressed gene by means of RT-PCR in various tissues and have foun...

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Veröffentlicht in:	Human molecular genetics 1993-04, Vol.2 (4), p.399-404
Hauptverfasser:	Verkerk, Annemieke J.M.H., de Graaff, Esther, De Boulle, Kristel, Eichler, Evan E., Konecki, David S., Reyniers, Edwin, Manca, Antonella, Poustka, Annemarie, Willems, Patrick J., Nelson, David L., Oostra, Ben A.
Format:	Artikel
Sprache:	eng
Schlagworte:	Alternative Splicing - genetics Amino Acid Sequence Base Sequence Biological and medical sciences cDNA Chromosome fragility (bloom syndrome, ataxia telangiectasia, fanconi anemia, x-linked mental retardation...) DNA - genetics DNA Mutational Analysis Exons FMR1 gene fragile sites Fragile X Syndrome - genetics genes Humans Introns Male man Medical genetics Medical sciences Molecular Sequence Data nucleotide sequence Polymerase Chain Reaction RNA, Messenger - genetics splicing Transcription, Genetic
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