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Q24630545-3DE820E5-9712-4DB2-A5B6-CCEF0440FC6D
Q24630545-3DE820E5-9712-4DB2-A5B6-CCEF0440FC6D
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http://www.wikidata.org/entity/statement/Q24630545-3DE820E5-9712-4DB2-A5B6-CCEF0440FC6D
Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss
P2860
Q24630545-3DE820E5-9712-4DB2-A5B6-CCEF0440FC6D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24630545-3DE820E5-9712-4DB2-A5B6-CCEF0440FC6D
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wasDerivedFrom
b26fccc8857b85a0e7b0653ab776dd9b40e50857
P2860
Mutations in the SPTLC2 subunit of serine palmitoyltransferase cause hereditary sensory and autonomic neuropathy type I