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Q47671849-42FA8A7F-0129-470B-8407-069B2F6A5971
Q47671849-42FA8A7F-0129-470B-8407-069B2F6A5971
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47671849-42FA8A7F-0129-470B-8407-069B2F6A5971
Ultrastructural Immunocytochemical Abnormalities of Peripheral Myelin Proteins in Hereditary Sensory-Motor Neuropathies: 12 cases.
P2860
Q47671849-42FA8A7F-0129-470B-8407-069B2F6A5971
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47671849-42FA8A7F-0129-470B-8407-069B2F6A5971
rank
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type
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Statement
wasDerivedFrom
ae2b24a13c1330658ba5664139f1fbb07f016c92
P2860
Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research Group.