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Q24685930-345F221E-A915-435F-9167-A27459A89D3B
Q24685930-345F221E-A915-435F-9167-A27459A89D3B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24685930-345F221E-A915-435F-9167-A27459A89D3B
A compound heterozygous one amino-acid insertion/nonsense mutation in the plectin gene causes epidermolysis bullosa simplex with plectin deficiency
P2860
Q24685930-345F221E-A915-435F-9167-A27459A89D3B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24685930-345F221E-A915-435F-9167-A27459A89D3B
rank
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type
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Statement
wasDerivedFrom
07a368733fd6c12005fcab214ed5595e9e3b1e09
P2860
Myopathy, myasthenic syndrome, and epidermolysis bullosa simplex due to plectin deficiency