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A Rapid and Sensitive PCR Screening Method for Point Mutations Associated with Mitochondrial Encephalomyopathies

✍ Scribed by P. Seibel; A. Flierl; M. Kottlors; H. Reichmann


Book ID
115574572
Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
258 KB
Volume
200
Category
Article
ISSN
0006-291X

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Communicated by Cha& I. Epstein More than 150 mutations in the genes for type I procollagein have been found in unrelated patients with osteogenesis imperfecta (01), but mutations have been difficult to define in many patients with the mildest forms of the disease. Here, we have used robotically aut