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Cracking rare disorders: a new minimally invasive RNA-seq protocol by Laurenz De Cock, Erika D’haenens, Lies Vantomme, Lynn Backers, Aude Beyens, Kathleen BM Claes, Griet De Clercq, Robin de Putter, Candy Kumps, Nika Schuermans, Jo Sourbron, Hannes Syryn, Simon Tavernier, Eva Vanbelleghem, Olivier Vanakker, Bart Vandekerckhove, Tim Van Damme, Bert Callewaert, Annelies Dheedene, Sarah Vergult, Björn Menten
Published 2025-05-01Get full text
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P321: Identifying new genotype/phenotype correlations for individuals carrying deleterious RERE variants by David Curtis, Daryl Scott, Seema Lalani, Mahshid Azamian, Kierstin Keller, Alanna Strong, Joseph Shen, Colette DeFilippo, Himanshu Goel, Betsy Schmalz, Bimal Chaudhari, Shelagh Joss, Muge Gucsavas-Calikoglu, Yael Shiloh-Malawsky, Yezmin Perilla-Young, Olivia Thompson, Neena Champaigne, Luigi Chiratti, Marco Ferilli, Marco Tartaglia, Manuela Priolo, Radio Clementina, Christelle Achkar, Koen Gassen, Marie-José van den Boogard, Tony Roscioli, Kim McBride, Julie Lauzon, Hannes Syryn, Martine Cools, Elfride De Baere, Victor Faundes, Gabriela Repetto, Sarah Josephi-Taylor, Adam Bournazos, Sandra Cooper, Nichole Owen, Xiaonan Zhao
Published 2025-01-01Get full text
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