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Q52839213-805045B8-3D1A-4DBD-BF22-D1104099B51C
Q52839213-805045B8-3D1A-4DBD-BF22-D1104099B51C
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http://www.wikidata.org/entity/statement/Q52839213-805045B8-3D1A-4DBD-BF22-D1104099B51C
Diagnostic whole genome sequencing and split-read mapping for nucleotide resolution breakpoint identification in CNTNAP2 deficiency syndrome.
P2860
Q52839213-805045B8-3D1A-4DBD-BF22-D1104099B51C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52839213-805045B8-3D1A-4DBD-BF22-D1104099B51C
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wasDerivedFrom
30e481ca0c61a93a5f44fff099f8a3c8bc83f516
P2860
CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila