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Q36325792-7895D2E3-F4DB-4160-9D12-AE3AA5753BA8
Q36325792-7895D2E3-F4DB-4160-9D12-AE3AA5753BA8
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http://www.wikidata.org/entity/statement/Q36325792-7895D2E3-F4DB-4160-9D12-AE3AA5753BA8
Mitochondrial Dysfunction in a Patient with 8q21.11 Deletion and Charcot-Marie-Tooth Disease Type 2K due to GDAP1 Haploinsufficiency.
P2860
Q36325792-7895D2E3-F4DB-4160-9D12-AE3AA5753BA8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36325792-7895D2E3-F4DB-4160-9D12-AE3AA5753BA8
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wasDerivedFrom
68a9abe29c1f3f4e4a84d398842a498e9b1577b5
P2860
Dominant GDAP1 mutations cause predominantly mild CMT phenotypes