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Q45107853-0ECAA17D-4957-426B-AEF5-B1AB56C4ACCE
Q45107853-0ECAA17D-4957-426B-AEF5-B1AB56C4ACCE
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http://www.wikidata.org/entity/statement/Q45107853-0ECAA17D-4957-426B-AEF5-B1AB56C4ACCE
Mutation analysis of MFN2, GJB1, MPZ and PMP22 in Italian patients with axonal Charcot-Marie-Tooth disease.
P2860
Q45107853-0ECAA17D-4957-426B-AEF5-B1AB56C4ACCE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q45107853-0ECAA17D-4957-426B-AEF5-B1AB56C4ACCE
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wasDerivedFrom
554e0d430b35db486b815a56f7f25ebbbf6b10eb
P2860
Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A.