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Q37089623-3CDFF66E-DE71-46E4-AF82-B3E517C0F9DC
Q37089623-3CDFF66E-DE71-46E4-AF82-B3E517C0F9DC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37089623-3CDFF66E-DE71-46E4-AF82-B3E517C0F9DC
hnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndrome
P356
Q37089623-3CDFF66E-DE71-46E4-AF82-B3E517C0F9DC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37089623-3CDFF66E-DE71-46E4-AF82-B3E517C0F9DC
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
37f77e0ed667969911e7dc86f13c5fc2393f533e
P356
10.1093/HMG/DDN305
http://www.w3.org/2001/XMLSchema#string
P356
DDN305