Andreas Roos
5PUBLICATIONS
5CO-AUTHORS
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Publications (5)
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|Mar 21, 2023
Correction: A Homozygous PPP1R21 Splice Variant Associated with Severe Developmental Delay, Absence of Speech, and Muscle Weakness Leads to Activated Proteasome Function.Andreas Hentschel, Nancy Meyer, Nicolai Kohlschmidt
|Jan 24, 2023
A Homozygous PPP1R21 Splice Variant Associated with Severe Developmental Delay, Absence of Speech, and Muscle Weakness Leads to Activated Proteasome Function.Andreas Hentschel, Nancy Meyer, Nicolai Kohlschmidt
|Feb 03, 2022
Identification of a novel homozygous synthesis of cytochrome c oxidase 2 variant in siblings with early-onset axonal Charcot-Marie-Tooth disease.Andrea Gangfuß, Andreas Hentschel, Nina Rademacher
|Feb 01, 2022
Novel insights into PORCN mutations, associated phenotypes and pathophysiological aspects.Annabelle Arlt, Nicolai Kohlschmidt, Andreas Hentschel
|Feb 10, 2021
Protein signature of human skin fibroblasts allows the study of the molecular etiology of rare neurological diseases.Andreas Hentschel, Artur Czech, Ute Münchberg
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