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An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus
Genomics · 1988 · Vol. 2(1) · pp. 90–95
Anthony P. Monaco✉(Boston Children's Hospital)Corlee J. Bertelson(Harvard University)Sabina Liechti‐Gallati(Swiss National Science Foundation)Hans Moser(University Hospital of Bern)Louis M. Kunkel(Harvard University)
Muscle Physiology and DisordersRNA Research and SplicingCRISPR and Genetic EngineeringBiologyGeneticsLocus (genetics)GeneOpen reading framePhenotypeDuchenne muscular dystrophyAmino acidGene productMuscular dystrophy
MeSH terms
AdolescentAdultBase SequenceChromosome DeletionExonsGenesHumansMaleMolecular Sequence DataMuscular DystrophiesPhenotype
Funding
- National Institutes of Health
Citations
1,186
FWCI
13.87
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32
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99%
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Cited by
Variants of the DMD gene in 18 patients, clinical severity prediction, genotype-phenotype correlation, and potential therapies
International Journal of Advanced Research in Medicine · 2022 · 0 citations
References
Organization and Expression of Eucaryotic Split Genes Coding for Proteins
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Lambda replacement vectors carrying polylinker sequences
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Detection of specific sequences among DNA fragments separated by gel electrophoresis
Journal of Molecular Biology · 1975 · 32,825 citations
Dystrophin: The protein product of the duchenne muscular dystrophy locus
Cell · 1987 · 4,654 citations
DNA sequencing with chain-terminating inhibitors
Proceedings of the National Academy of Sciences · 1977 · 69,196 citations
The pUC plasmids, an M13mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primers
Gene · 1982 · 6,131 citations
Construction and characterization of new cloning vehicle. II. A multipurpose cloning system
Gene · 1977 · 3,858 citations
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