Found: 1

Select item for more details and to access through your institution.

  • CHEDDA syndrome is an underrecognized neurodevelopmental disorder with a highly restricted ATN1 mutation spectrum.

    Published in:
    Clinical Genetics, 2021, v. 100, n. 4, p. 468, doi. 10.1111/cge.14022
    By:
    • Palmer, Elizabeth E.;
    • Whitton, Chloe;
    • Hashem, Mais O.;
    • Clark, Robin D.;
    • Ramanathan, Subhadra;
    • Starr, Lois J.;
    • Velasco, Danita;
    • De Dios, John Karl;
    • Singh, Emily;
    • Cormier‐Daire, Valerie;
    • Chopra, Maya;
    • Rodan, Lance H.;
    • Nellaker, Christoffer;
    • Lakhani, Shenela;
    • Mallack, Eric J.;
    • Panzer, Karin;
    • Sidhu, Alpa;
    • Wentzensen, Ingrid M.;
    • Lacombe, Didier;
    • Michaud, Vincent
    Publication type:
    Article