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Q36477658-4CED18F2-5554-4B4B-92CC-B435BCE18163
Q36477658-4CED18F2-5554-4B4B-92CC-B435BCE18163
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http://www.wikidata.org/entity/statement/Q36477658-4CED18F2-5554-4B4B-92CC-B435BCE18163
Mutation analysis of CHRNA1, CHRNB1, CHRND, and RAPSN genes in multiple pterygium syndrome/fetal akinesia patients.
P2860
Q36477658-4CED18F2-5554-4B4B-92CC-B435BCE18163
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36477658-4CED18F2-5554-4B4B-92CC-B435BCE18163
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wasDerivedFrom
48f484b8dadb488d941632be7077477f588a0c7b
P2860
Rapsyn mutations in humans cause endplate acetylcholine-receptor deficiency and myasthenic syndrome