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EJHG.2011.261
EJHG.2011.261
http://dx.doi.org/10.1038/EJHG.2011.261
KIF1A missense mutations in SPG30, an autosomal recessive spastic paraplegia: distinct phenotypes according to the nature of the mutations
P356
Q35969072-84EF106D-3FFC-4B0D-80B6-B0FD39843ECF
P356
EJHG.2011.261
http://dx.doi.org/10.1038/EJHG.2011.261