Publications by authors named "Kerstin Alt"

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Biallelic variants in PIGN cause Fryns syndrome, multiple congenital anomalies-hypotonia-seizures syndrome, and neurologic phenotypes: A genotype-phenotype correlation study.
Lucy Loong, Agostina Tardivo, Alexej Knaus, Mona Hashim, Alistair T Pagnamenta, Kerstin Alt

Genet Med· January 2023

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PIGN encephalopathy: Characterizing the epileptology.
Allan Bayat, Guillem de Valles-Ibáñez, Manuela Pendziwiat, Alexej Knaus, Kerstin Alt

Epilepsia· April 2022

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NR4A2 and Dystonia with Dopa Responsiveness.
Benedikt Winter, Johannes Krämer, Tamara Meinhardt, Daniel Berner, Kerstin Alt

Mov Disord· September 2021

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Camptocormia as a Novel Phenotype in a Heterozygous Mutation.
Diana Lehmann Urban, Leila Motlagh Scholle, Kerstin Alt, Albert C Ludolph, Angela Rosenbohm

Diagnostics (Basel)· January 2020

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CRISPR/Cas9-Mediated Knockout of MicroRNA-744 Improves Antibody Titer of CHO Production Cell Lines.
Nadja Raab, Sven Mathias, Kerstin Alt, René Handrick, Simon Fischer

Biotechnol J· May 2019

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