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Q50420610-20853E23-7D18-4142-B764-97F7AABBB8B9
Q50420610-20853E23-7D18-4142-B764-97F7AABBB8B9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50420610-20853E23-7D18-4142-B764-97F7AABBB8B9
Phenotype of CNTNAP1: a study of patients demonstrating a specific severe congenital hypomyelinating neuropathy with survival beyond infancy.
P2860
Q50420610-20853E23-7D18-4142-B764-97F7AABBB8B9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50420610-20853E23-7D18-4142-B764-97F7AABBB8B9
rank
NormalRank
type
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Statement
wasDerivedFrom
d59db0e2447c50f8b21c056bb1293ab77885d97c
P2860
Whole exome sequencing in patients with white matter abnormalities.