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Q37089623-3386E41D-617C-4877-8B71-F23141BC18B0
Q37089623-3386E41D-617C-4877-8B71-F23141BC18B0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37089623-3386E41D-617C-4877-8B71-F23141BC18B0
hnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndrome
P2860
Q37089623-3386E41D-617C-4877-8B71-F23141BC18B0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37089623-3386E41D-617C-4877-8B71-F23141BC18B0
rank
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wasDerivedFrom
62a07d2b1970706b007c939bed19f64e564d0d3e
P2860
Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism