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Q39273628-D0437E4E-014F-45E4-A7A8-94330DF4F5EF
Q39273628-D0437E4E-014F-45E4-A7A8-94330DF4F5EF
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Statement
http://www.wikidata.org/entity/statement/Q39273628-D0437E4E-014F-45E4-A7A8-94330DF4F5EF
Human diseases associated with connexin mutations.
P2860
Q39273628-D0437E4E-014F-45E4-A7A8-94330DF4F5EF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39273628-D0437E4E-014F-45E4-A7A8-94330DF4F5EF
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wasDerivedFrom
0d61b3900f1f523feeeabe497ca6a491d872d808
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.