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Q43779485-F999E96F-5B6F-4504-99A2-58F27FE151EE
Q43779485-F999E96F-5B6F-4504-99A2-58F27FE151EE
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Statement
http://www.wikidata.org/entity/statement/Q43779485-F999E96F-5B6F-4504-99A2-58F27FE151EE
Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1).
P31
Q43779485-F999E96F-5B6F-4504-99A2-58F27FE151EE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q43779485-F999E96F-5B6F-4504-99A2-58F27FE151EE
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type
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wasDerivedFrom
36329b6c828850b75b5f14b0333300f2d261ddbc
P31
scholarly article