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Q33646656-5ED1CAE7-D44D-42BF-864C-5899BCEB3B15
Q33646656-5ED1CAE7-D44D-42BF-864C-5899BCEB3B15
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http://www.wikidata.org/entity/statement/Q33646656-5ED1CAE7-D44D-42BF-864C-5899BCEB3B15
Clinical and Genetic Features of Chinese X-linked Charcot-Marie-Tooth Type 1 Disease.
P2860
Q33646656-5ED1CAE7-D44D-42BF-864C-5899BCEB3B15
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33646656-5ED1CAE7-D44D-42BF-864C-5899BCEB3B15
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wasDerivedFrom
93ba58bd24368dbd0307caf6326db39391836ab4
P2860
Compound Heterozygote Mutation of C12orf65 Causes Distal Motor Neuropathy and Optic Atrophy