Phenotype variability in patients with infantile spinal muscular atrophy: Distal muscle weakness and peripheral neuropathy in compound heterozygotes with SMN1 gene deletions
Barisic, N, Grdjan, P, Lehman, I, Sertic, J, Cvitanovic-Sojat, L.J, Jakovcevic, A, Rudnik-Schöneborn, S
Published in European journal of paediatric neurology (01.06.2017)
Published in European journal of paediatric neurology (01.06.2017)
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