Mutations at a split codon in the GTPase-encoding domain of OPA1 cause dominant optic atrophy through different molecular mechanisms

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Mutations at a split codon in the GTPase-encoding domain of OPA1 cause dominant optic atrophy through different molecular mechanisms

Author: Weisschuh, Nicole; Marino, Valerio; Schaeferhoff, Karin; Richter, Paul; Park, Joohyun; Haack, Tobias B.; Dell'Orco, Daniele
Tübinger Autor(en):
Weisschuh, Nicole
Richter, Paul
Park, Joohyun
Schäferhoff, Karin
Haack, Tobias
Published in: Human Molecular Genetics (2022), Bd. 31, H. 5, S. 761-774
Verlagsangabe: Oxford Univ Press
Language: English
Full text: http://dx.doi.org/10.1093/hmg/ddab286
ISSN: 0964-6906
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Article
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