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Q34995414-DA1044D7-2092-488D-8BAF-57227FAEB54D
Q34995414-DA1044D7-2092-488D-8BAF-57227FAEB54D
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http://www.wikidata.org/entity/statement/Q34995414-DA1044D7-2092-488D-8BAF-57227FAEB54D
Genes for hereditary sensory and autonomic neuropathies: a genotype-phenotype correlation.
P2860
Q34995414-DA1044D7-2092-488D-8BAF-57227FAEB54D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34995414-DA1044D7-2092-488D-8BAF-57227FAEB54D
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wasDerivedFrom
4085e61ddb03e73f9d390cf776104acc9ec171b3
P2860
Mutation in the epsilon subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic paraplegia.