An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus

Deletions giving rise to Duchenne muscular dystrophy (DMD) and the less severe Becker muscular dystrophy (BMD) occur in the same large gene on the short arm of the human X chromosome. We present a molecular mechanism to explain the clinical difference in serity between DMD and BMD patients who bear...

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Veröffentlicht in:	Genomics (San Diego, Calif.) Calif.), 1988, Vol.2 (1), p.90-95
Hauptverfasser:	Monaco, Anthony P., Bertelson, Corlee J., Liechti-Gallati, Sabina, Moser, Hans, Kunkel, Louis M.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Base Sequence Chromosome Deletion Exons Genes Humans Male Molecular Sequence Data Muscular Dystrophies - genetics Phenotype
Online-Zugang:	Volltext
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