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Q48116911-069850BF-642C-42BD-998B-9F1BBF13A58A
Q48116911-069850BF-642C-42BD-998B-9F1BBF13A58A
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http://www.wikidata.org/entity/statement/Q48116911-069850BF-642C-42BD-998B-9F1BBF13A58A
Reply: The phenotypic and molecular spectrum of PEHO syndrome and PEHO-like disorders.
P2860
Q48116911-069850BF-642C-42BD-998B-9F1BBF13A58A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48116911-069850BF-642C-42BD-998B-9F1BBF13A58A
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52d8b12ea3b94b64dd6c06a0c7fcc757523e2e29
P2860
Biallelic Mutations in TBCD, Encoding the Tubulin Folding Cofactor D, Perturb Microtubule Dynamics and Cause Early-Onset Encephalopathy