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Q24654250-50B5B88B-1863-4C70-8E5D-3433E8BFBEF2
Q24654250-50B5B88B-1863-4C70-8E5D-3433E8BFBEF2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24654250-50B5B88B-1863-4C70-8E5D-3433E8BFBEF2
Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations
P2860
Q24654250-50B5B88B-1863-4C70-8E5D-3433E8BFBEF2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24654250-50B5B88B-1863-4C70-8E5D-3433E8BFBEF2
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Statement
wasDerivedFrom
98be6ed244cf3b544fd6abd44a85df2297af20fc
P2860
Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease