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Q34399213-E7EAB26E-B692-443B-A505-56E6FE8C2EC5
Q34399213-E7EAB26E-B692-443B-A505-56E6FE8C2EC5
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http://www.wikidata.org/entity/statement/Q34399213-E7EAB26E-B692-443B-A505-56E6FE8C2EC5
Clinical and genetic diversity of SMN1-negative proximal spinal muscular atrophies
P2860
Q34399213-E7EAB26E-B692-443B-A505-56E6FE8C2EC5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34399213-E7EAB26E-B692-443B-A505-56E6FE8C2EC5
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wasDerivedFrom
08e73f1406d5766637fd9fc99b4de7164d3086de
P2860
Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegia