Heterozygous CELF4 variants in the N-term region crucial for the RNA-binding activity lead to neurodevelopmental disorder and obesity

Related articles

1. Saturation genome editing of RNU4-2 reveals distinct dominant and recessive neurodevelopmental disorders

   This article has 42 authors:

   1. Joachim De Jonghe
   2. Hyung Chul Kim
   3. Ayanfeoluwa Adedeji
   4. Elsa Leitão
   5. Ruebena Dawes
   6. Yuyang Chen
   7. Alexander JM Blakes
   8. Cas Simons
   9. Rocio Rius
   10. Javeria R Alvi
   11. Florence Amblard
   12. Christina Austin-Tse
   13. Sarah Baer
   14. Elsa V Balton
   15. Pierre Blanc
   16. Daniel G Calame
   17. Charles Coutton
   18. Chloe A Cunningham
   19. Nitsuh Dargie
   20. Katrina M Dipple
   21. Haowei Du
   22. Salima El Chehadeh
   23. Ian Glass
   24. Joseph G Gleeson
   25. Olivier Grunewald
   26. Paul Gueguen
   27. Radu Harbuz
   28. Marie-Line Jacquemont
   29. Richard J Leventer
   30. Pierre Marijon
   31. Olfa Messaoud
   32. Tipu Sultan
   33. Christel Thauvin
   34. Catherine Vincent-Delorme
   35. Elif Yilmaz Gulec
   36. Julien Thevenon
   37. Rodrigo Mendez
   38. Daniel G MacArthur
   39. Christel Depienne
   40. Caroline Nava
   41. Nicola Whiffin
   42. Gregory M Findlay

2. Targeted long-read RNA sequencing reveals the complexity of CLN3 transcription and the consequences of the most common 1-kb deletion in patients with juvenile CLN3 disease

   This article has 17 authors:

   1. Christopher J Minnis
   2. Hao-Yu Zhang
   3. Emil Gustavsson
   4. Jasmaine Lee
   5. Claire Anderson
   6. Emily Gardner
   7. Angela Schulz
   8. Miriam Nickel
   9. Gavin Arno
   10. Neringa Jurkute
   11. Andrew R Webster
   12. Nicola Gammaldi
   13. Filippo M Santorelli
   14. Paul Gissen
   15. Phillipa Mills
   16. Mina Ryten
   17. Sara E Mole

3. Psmd13, a proteosome regulatory subunit identified in miR-29a regulation during neurogenesis

   This article has 3 authors:

   1. Diji Kuriakose
   2. Grant Morahan
   3. Zhicheng Xiao