Abstract:
:Large muscle genes are often sequenced using complementary DNA (cDNA) made from muscle messenger RNA (mRNA) to reduce the cost and workload associated with sequencing from genomic DNA. Two potential barriers are the availability of a frozen muscle biopsy, and difficulties in detecting nonsense mutations due to nonsense-mediated mRNA decay (NMD). We present patient examples showing that use of MyoD-transduced fibroblasts as a source of muscle-specific mRNA overcomes these potential difficulties in sequencing large muscle-related genes.
journal_name
Muscle Nervejournal_title
Muscle & nerveauthors
Waddell LB,Monnier N,Cooper ST,North KN,Clarke NFdoi
10.1002/mus.22118subject
Has Abstractpub_date
2011-08-01 00:00:00pages
280-2issue
2eissn
0148-639Xissn
1097-4598journal_volume
44pub_type
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