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A novel de novo mutation in the triple helix of the COL6A3 gene in a two-generation Italian family affected by Bethlem myopathy. A diagnostic approach in the mutations' screening of type VI collagen. [electronic resource] by
- Pepe, G
- Bertini, E
- Giusti, B
- Brunelli, T
- Comeglio, P
- Saitta, B
- Merlini, L
- Chu, M L
- Federici, G
- Abbate, R
Producer: 19990901
In:
Neuromuscular disorders : NMD vol. 9
Availability: No items available.
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