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BioMed Central, BMC Medical Genetics, 1(14), 2013
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Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1 gene C-Terminal domain: a case report
Journal article published in 2013 by
Elena Martoni,
Stefania Petrini,
Cecilia Trabanelli,
Patrizia Sabatelli,
Anna Urciuolo,
Rita Selvatici 
,
Adele D'Amico,
Sofia Falzarano,
Enrico Bertini,
Paolo Bonaldo,
Alessandra Ferlini,
Francesca Gualandi
,
Adele D'Amico,
Sofia Falzarano,
Enrico Bertini,
Paolo Bonaldo,
Alessandra Ferlini,
Francesca Gualandi
This paper is made freely available by the publisher.
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