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Q27335461-CE49DECF-B73A-46EE-8EFA-91E3B97BC604
Q27335461-CE49DECF-B73A-46EE-8EFA-91E3B97BC604
BestRank
Statement
http://www.wikidata.org/entity/statement/Q27335461-CE49DECF-B73A-46EE-8EFA-91E3B97BC604
Targeted proteolysis of plectin isoform 1a accounts for hemidesmosome dysfunction in mice mimicking the dominant skin blistering disease EBS-Ogna
P2860
Q27335461-CE49DECF-B73A-46EE-8EFA-91E3B97BC604
BestRank
Statement
http://www.wikidata.org/entity/statement/Q27335461-CE49DECF-B73A-46EE-8EFA-91E3B97BC604
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wasDerivedFrom
3cb388125514d89c6e421d28846f348c93d3598c
P2860
Mutation in exon 1f of PLEC, leading to disruption of plectin isoform 1f, causes autosomal-recessive limb-girdle muscular dystrophy