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[1]
C. Kim,et al.
New insights in mucopolysaccharidosis type VI: Neurological perspective
,
2014,
Brain and Development.
[2]
P. Harmatz,et al.
Craniocervical decompression in patients with mucopolysaccharidosis VI: development of a scoring system to determine indication and outcome of surgery
,
2013,
Journal of Inherited Metabolic Disease.
[3]
B. Burton,et al.
A multinational, multidisciplinary consensus for the diagnosis and management of spinal cord compression among patients with mucopolysaccharidosis VI.
,
2012,
Molecular genetics and metabolism.
[4]
D. Horovitz,et al.
Spinal cord compression in young children with type VI mucopolysaccharidosis.
,
2011,
Molecular genetics and metabolism.