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GestaltMatcher Database - A global reference for the facial phenotypic variability of rare human diseases.
medRxiv [Preprint]. 2024 Mar 8:2023.06.06.23290887. doi: 10.1101/2023.06.06.23290887.
medRxiv. 2024.
PMID: 37503210
Free PMC article.
Preprint.
Molecular and Functional Characterization of BDNF-Overexpressing Human Retinal Pigment Epithelial Cells Established by Sleeping Beauty Transposon-Mediated Gene Transfer.
Mattern L, Otten K, Miskey C, Fuest M, Izsvák Z, Ivics Z, Walter P, Thumann G, Johnen S.
Mattern L, et al.
Int J Mol Sci. 2022 Oct 26;23(21):12982. doi: 10.3390/ijms232112982.
Int J Mol Sci. 2022.
PMID: 36361771
Free PMC article.
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Variant of the catalytic cysteine of UFSP2 leads to spondyloepimetaphyseal dysplasia type Di Rocco.
Mattern L, Begemann M, Delbrück H, Holschbach P, Schröder S, Schacht SM, Kurth I, Elbracht M.
Mattern L, et al.
Bone Rep. 2023 May 4;18:101683. doi: 10.1016/j.bonr.2023.101683. eCollection 2023 Jun.
Bone Rep. 2023.
PMID: 37214758
Free PMC article.
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