Dystrophin nonsense mutation induces different levels of exon 29 skipping and leads to variable phenotypes within one BMD family - Concepedia

Concepedia

Publication | Open Access

Dystrophin nonsense mutation induces different levels of exon 29 skipping and leads to variable phenotypes within one BMD family

DOI Full Paper Access

87

Citations

18

References

2000

Year

Ieke B. Ginjaar, Alexander L.J. Kneppers, Jan-Douwe M v d Meulen, Louise V.B. Anderson, Mattie Bremmer-Bout, Judith C. van Deutekom, Jitske Weegenaar, Johan T. den Dunnen, Egbert Bakker

European Journal of Human Genetics

Mendelian DisorderGenetic DisorderGeneticsVariable PhenotypesPathologyDegenerative DiseaseMolecular GeneticsDisease Gene IdentificationMedicineBmd Family

References

	Year	Citations

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