TY  - GEN
AU  - Mercuri,E
AU  - Messina,S
AU  - Bruno,C
AU  - Mora,M
AU  - Pegoraro,E
AU  - Comi,G P
AU  - D'Amico,A
AU  - Aiello,C
AU  - Biancheri,R
AU  - Berardinelli,A
AU  - Boffi,P
AU  - Cassandrini,D
AU  - Laverda,A
AU  - Moggio,M
AU  - Morandi,L
AU  - Moroni,I
AU  - Pane,M
AU  - Pezzani,R
AU  - Pichiecchio,A
AU  - Pini,A
AU  - Minetti,C
AU  - Mongini,T
AU  - Mottarelli,E
AU  - Ricci,E
AU  - Ruggieri,A
AU  - Saredi,S
AU  - Scuderi,C
AU  - Tessa,A
AU  - Toscano,A
AU  - Tortorella,G
AU  - Trevisan,C P
AU  - Uggetti,C
AU  - Vasco,G
AU  - Santorelli,F M
AU  - Bertini,E
TI  - Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study
SN  - 1526-632X
PY  - 2009///0625
KW  - Adolescent
KW  - Brain
KW  - pathology
KW  - Child
KW  - Child, Preschool
KW  - Cohort Studies
KW  - Dystroglycans
KW  - analysis
KW  - Female
KW  - Glycosylation
KW  - Glycosyltransferases
KW  - genetics
KW  - Humans
KW  - Infant
KW  - Italy
KW  - Magnetic Resonance Imaging
KW  - Mannosyltransferases
KW  - Membrane Proteins
KW  - Muscle, Skeletal
KW  - chemistry
KW  - Muscular Dystrophies
KW  - congenital
KW  - Mutation
KW  - N-Acetylglucosaminyltransferases
KW  - Pentosyltransferases
KW  - Phenotype
KW  - Prevalence
KW  - Proteins
N1  - Publication Type: Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1212/01.wnl.0000346518.68110.60
ER  -