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ENE.12937
ENE.12937
http://dx.doi.org/10.1111/ENE.12937
A founder mutation p.H701P identified as a major cause of SPG7 in Norway.
P356
Q53323741-1A9DC029-4408-4B72-8908-59104797141F
P356
ENE.12937
http://dx.doi.org/10.1111/ENE.12937