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SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype.
Am J Hum Genet. 2021 Nov 4;108(11):2112-2129. doi: 10.1016/j.ajhg.2021.09.007. Epub 2021 Oct 8.
Am J Hum Genet. 2021.
PMID: 34626534
Free PMC article.
Serotonin-specific neurons differentiated from human iPSCs form distinct subtypes with synaptic protein assembly.
Jansch C, Ziegler GC, Forero A, Gredy S, Wäldchen S, Vitale MR, Svirin E, Zöller JEM, Waider J, Günther K, Edenhofer F, Sauer M, Wischmeyer E, Lesch KP.
Jansch C, et al. Among authors: gredy s.
J Neural Transm (Vienna). 2021 Feb;128(2):225-241. doi: 10.1007/s00702-021-02303-5. Epub 2021 Feb 9.
J Neural Transm (Vienna). 2021.
PMID: 33560471
Free PMC article.
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Genotype- and Age-Dependent Differences in Ultrasound Vocalizations of SPRED2 Mutant Mice Revealed by Machine Deep Learning.
Hepbasli D, Gredy S, Ullrich M, Reigl A, Abeßer M, Raabe T, Schuh K.
Hepbasli D, et al. Among authors: gredy s.
Brain Sci. 2021 Oct 17;11(10):1365. doi: 10.3390/brainsci11101365.
Brain Sci. 2021.
PMID: 34679429
Free PMC article.
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