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1
Q36338162-E0A039F8-124B-4CED-AE52-BCE1A5BE70F1
Q36338162-E0A039F8-124B-4CED-AE52-BCE1A5BE70F1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36338162-E0A039F8-124B-4CED-AE52-BCE1A5BE70F1
A recurrent deletion syndrome at chromosome bands 2p11.2-2p12 flanked by segmental duplications at the breakpoints and including REEP1
P2860
Q36338162-E0A039F8-124B-4CED-AE52-BCE1A5BE70F1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36338162-E0A039F8-124B-4CED-AE52-BCE1A5BE70F1
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
98c1d12e82ae76a9b592aa85998514411b23f1a2
P2860
REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31.