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Q35097544-0A4D2562-0B0C-48BA-A0B7-7FEAF68AC81B
Q35097544-0A4D2562-0B0C-48BA-A0B7-7FEAF68AC81B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35097544-0A4D2562-0B0C-48BA-A0B7-7FEAF68AC81B
Genomic medicine and neurological disease.
P2860
Q35097544-0A4D2562-0B0C-48BA-A0B7-7FEAF68AC81B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35097544-0A4D2562-0B0C-48BA-A0B7-7FEAF68AC81B
rank
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Statement
wasDerivedFrom
23dc787fd66e705a09c5b32f388ebd26e2bf91bc
P2860
Mutation in exon 1f of PLEC, leading to disruption of plectin isoform 1f, causes autosomal-recessive limb-girdle muscular dystrophy