DOI:
10.1055/s-00000041
Neuropediatrics
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References
Vieira NM, Schlesinger D, de Paula F, Vainzof M, Zatz M.
Mutation analysis in the FKRP gene provides an explanation for a rare cause of intrafamilial clinical variability in LGMD2I.
Neuromuscul Disord 2006;
16 (12) 870-873
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