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Q24309219-16B08FAC-23BE-4BB6-974F-0D4114F871E4
Q24309219-16B08FAC-23BE-4BB6-974F-0D4114F871E4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24309219-16B08FAC-23BE-4BB6-974F-0D4114F871E4
Mutation in exon 1f of PLEC, leading to disruption of plectin isoform 1f, causes autosomal-recessive limb-girdle muscular dystrophy
P2860
Q24309219-16B08FAC-23BE-4BB6-974F-0D4114F871E4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24309219-16B08FAC-23BE-4BB6-974F-0D4114F871E4
rank
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type
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wasDerivedFrom
248296e2ea50caaec4e59a3d03f783c0ba311778
P2860
ALX4 dysfunction disrupts craniofacial and epidermal development