Published in
Elsevier, Neuromuscular Disorders, 4(9), p. 264-271
DOI: 10.1016/s0960-8966(99)00014-0
Links
Tools
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
Journal article published in 1999 by
G. Pepe,
E. Bertini,
B. Giusti 
,
T. Brunelli,
P. Comeglio,
B. Saitta,
L. Merlini ,
M. L. Chu,
G. Federici,
R. Abbate
,
T. Brunelli,
P. Comeglio,
B. Saitta,
L. Merlini ,
M. L. Chu,
G. Federici,
R. Abbate
This paper is available in a repository.
Full text: Download
Published version:
archiving forbidden
Data provided by 