POMGnT1 mutations in congenital muscular dystrophy: genotype-phenotype correlation and expanded clinical spectrum.
Biancheri R, Bertini E, Falace A, Pedemonte M, Rossi A, D'Amico A, Scapolan S, Bergamino L, Petrini S, Cassandrini D, Broda P, Manfredi M, Zara F, Santorelli FM, Minetti C, Bruno C.
Biancheri R, et al. Among authors: bergamino l.
Arch Neurol. 2006 Oct;63(10):1491-5. doi: 10.1001/archneur.63.10.1491.
Arch Neurol. 2006.
PMID: 17030669