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Q33768227-DF89BA14-78BB-43B1-A825-0C923CB53F29
Q33768227-DF89BA14-78BB-43B1-A825-0C923CB53F29
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33768227-DF89BA14-78BB-43B1-A825-0C923CB53F29
A novel mutation in LRSAM1 causes axonal Charcot-Marie-Tooth disease with dominant inheritance
P2860
Q33768227-DF89BA14-78BB-43B1-A825-0C923CB53F29
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33768227-DF89BA14-78BB-43B1-A825-0C923CB53F29
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wasDerivedFrom
0fd665b07bcdf089dd3698633ea0112e69bb8990
P2860
Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor