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Q33735478-2A60203A-6F74-43B9-8E11-1DBF1606A411
Q33735478-2A60203A-6F74-43B9-8E11-1DBF1606A411
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Statement
http://www.wikidata.org/entity/statement/Q33735478-2A60203A-6F74-43B9-8E11-1DBF1606A411
Familial bulbospinal neuronopathy with optic atrophy: a distinct entity
P2860
Q33735478-2A60203A-6F74-43B9-8E11-1DBF1606A411
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33735478-2A60203A-6F74-43B9-8E11-1DBF1606A411
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wasDerivedFrom
7121497f5270f9aebecaf6c53b30c77cdd5f6717
P2860
Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies.