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Q26823332-76FF0CD0-1361-4AFA-AC3A-CEF138B83906
Q26823332-76FF0CD0-1361-4AFA-AC3A-CEF138B83906
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26823332-76FF0CD0-1361-4AFA-AC3A-CEF138B83906
Gap junctions in inherited human disorders of the central nervous system.
P2860
Q26823332-76FF0CD0-1361-4AFA-AC3A-CEF138B83906
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26823332-76FF0CD0-1361-4AFA-AC3A-CEF138B83906
rank
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wasDerivedFrom
5c83972dc50a4b65b3c13ffc86ba592addb83d57
P2860
Functional alterations in gap junction channels formed by mutant forms of connexin 32: evidence for loss of function as a pathogenic mechanism in the X-linked form of Charcot-Marie-Tooth disease.