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Q48242777-4B25A451-F6EC-48BD-962C-22C73AAC7147
Q48242777-4B25A451-F6EC-48BD-962C-22C73AAC7147
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http://www.wikidata.org/entity/statement/Q48242777-4B25A451-F6EC-48BD-962C-22C73AAC7147
Muscle biopsy.
P2860
Q48242777-4B25A451-F6EC-48BD-962C-22C73AAC7147
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48242777-4B25A451-F6EC-48BD-962C-22C73AAC7147
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wasDerivedFrom
dccafb7293d9150dc619fce758a200d1cca5cc6f
P2860
Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect.