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Q37089623-0C518783-B2CE-48BF-B731-FAE3618E7572
Q37089623-0C518783-B2CE-48BF-B731-FAE3618E7572
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37089623-0C518783-B2CE-48BF-B731-FAE3618E7572
hnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndrome
P2860
Q37089623-0C518783-B2CE-48BF-B731-FAE3618E7572
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37089623-0C518783-B2CE-48BF-B731-FAE3618E7572
rank
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type
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Statement
wasDerivedFrom
c558b1fd7cd8820e023b00b47ca203c4198c9d70
P2860
Congenital myasthenic syndromes: I. Deficiency and short open-time of the acetylcholine receptor.