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Q36170468-2DC3EC88-58C0-4CD9-966F-58752B8B4CC0
Q36170468-2DC3EC88-58C0-4CD9-966F-58752B8B4CC0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36170468-2DC3EC88-58C0-4CD9-966F-58752B8B4CC0
Diagnosis by sequencing: correction of misdiagnosis from FSHD2 to LGMD2A by whole-exome analysis.
P2860
Q36170468-2DC3EC88-58C0-4CD9-966F-58752B8B4CC0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36170468-2DC3EC88-58C0-4CD9-966F-58752B8B4CC0
rank
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type
BestRank
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wasDerivedFrom
4698c44ffa15bb1b2f970cb7588320bd8a2ac21e
P2860
A unifying genetic model for facioscapulohumeral muscular dystrophy