Publications by authors named "Ina Gehweiler"

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Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia.
Matias Wagner, Daniel P S Osborn, Ina Gehweiler, Maike Nagel, Ulrike Ulmer

Nat Commun· October 2019

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Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia.
Mohammad Ali Farazi Fard, Adriana P Rebelo, Elena Buglo, Hamid Nemati, Hassan Dastsooz, Ina Gehweiler

Am J Hum Genet· June 2019

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Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia.
Mohammad Ali Farazi Fard, Adriana P Rebelo, Elena Buglo, Hamid Nemati, Hassan Dastsooz, Ina Gehweiler

Am J Hum Genet· April 2019

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