De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathies

Sathiya N. Manivannan, Jolien Roovers, Noor Smal, Candace T. Myers, Dilsad Turkdogan, Filip Roelens, Oguz Kanca, Hyung Lok Chung, Tasja Scholz, Katharina Hermann, Tatjana Bierhals, Hande S. Caglayan, Hannah Stamberger, Dana Craiu, Carol Davila, Ingo Helbig, Renzo Guerrini, Anna Elina Lehesjoki, Carla Marini, Hiltrud MuhleRikke S. Møller, Bernd Neubauer, Deb Pal, Katalin Sterbova, Pasquale Striano, Tiina Talvik, Sarah Von Spiczak, Yvonne Weber, Dorota Hoffman-Zacharska, Heather Mefford, Peter De Jonghe, Shinya Yamamoto, Sarah Weckhuysen, Hugo J. Bellen

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Fingerprint

Dive into the research topics of 'De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathies'. Together they form a unique fingerprint.

Biochemistry, Genetics and Molecular Biology

Keyphrases