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Q30495383-1D1C5CB4-1F4F-4668-888C-7979B471334E
Q30495383-1D1C5CB4-1F4F-4668-888C-7979B471334E
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Statement
http://www.wikidata.org/entity/statement/Q30495383-1D1C5CB4-1F4F-4668-888C-7979B471334E
Mouse homologues of human hereditary disease.
P2860
Q30495383-1D1C5CB4-1F4F-4668-888C-7979B471334E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30495383-1D1C5CB4-1F4F-4668-888C-7979B471334E
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wasDerivedFrom
3889b553934eab2b0e702a3caff290267855ad38
P2860
Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A.