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Journal article

Molecular genetics of Duchenne muscular dystrophy.

Abstract:

The use of random fragments of DNA from a defined region of the human X chromosome has led to the identification of a region of DNA that exhibits deletion in patients with DMD. The same region is tightly linked to the disorder in families segregating the disease. A systematic search of the region has failed to detect reproducible transcription in any of the tissues tested, including both human adult and fetal tissue. A possibly more simple and straightforward approach is to utilize nucleotide...

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Publication status:
Published

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Publisher copy:
10.1101/SQB.1986.051.01.041

Authors


Kunkel, LM More by this author
More by this author
Institution:
University of Oxford
Department:
Oxford, MSD, Clinical Medicine, WTC Human Genetics
Bertelson, CJ More by this author
Colletti, CA More by this author
Journal:
Cold Spring Harbor symposia on quantitative biology
Volume:
51 Pt 1
Issue:
1
Pages:
349-351
Publication date:
1986
DOI:
EISSN:
1943-4456
ISSN:
0091-7451
URN:
uuid:48633e64-a225-492f-975b-31a9827957ed
Source identifiers:
115662
Local pid:
pubs:115662

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