Works by Myllykoski, Matti


Results: 19
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    HIDEA syndrome is caused by biallelic, pathogenic, rare or founder P4HTM variants impacting the active site or the overall stability of the P4H‐TM protein.

    Published in:
    Clinical Genetics, 2022, v. 102, n. 5, p. 444, doi. 10.1111/cge.14203
    By:
    • Kraatari‐Tiri, Minna;
    • Soikkonen, Leila;
    • Myllykoski, Matti;
    • Jamshidi, Yalda;
    • Karimiani, Ehsan G.;
    • Komulainen‐Ebrahim, Jonna;
    • Kallankari, Hanna;
    • Mignot, Cyril;
    • Depienne, Christel;
    • Keren, Boris;
    • Nougues, Marie‐Christine;
    • Alsahlawi, Zahra;
    • Romito, Antonio;
    • Martini, Javier;
    • Toosi, Mehran B.;
    • Carroll, Christopher J.;
    • Tripolszki, Kornelia;
    • Bauer, Peter;
    • Uusimaa, Johanna;
    • Bertoli‐Avella, Aida M.
    Publication type:
    Article
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    Molecular structure and function of myelin protein P0 in membrane stacking.

    Published in:
    Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-018-37009-4
    By:
    • Raasakka, Arne;
    • Ruskamo, Salla;
    • Kowal, Julia;
    • Han, Huijong;
    • Baumann, Anne;
    • Myllykoski, Matti;
    • Fasano, Anna;
    • Rossano, Rocco;
    • Riccio, Paolo;
    • Bürck, Jochen;
    • Ulrich, Anne S.;
    • Stahlberg, Henning;
    • Kursula, Petri
    Publication type:
    Article
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