P436: A novel pathogenic variant in NALCN gene in a newborn with CLIFAHDD syndrome

• Burak Altintas,
• Nathaniel Jensen,
• Shao Ching Tu,
• Sara Pajouhanfar,
• Korre Fairman,
• Catherine Gooch

Affiliations

Burak Altintas

Department of Pediatrics, Division of Genetics and Genomic Medicine, Washington University School of Medicine, St. Louis, MO

Nathaniel Jensen

Department of Pediatrics, Division of Genetics and Genomic Medicine, Washington University School of Medicine, St. Louis, MO

Shao Ching Tu

Department of Pediatrics, Division of Genetics and Genomic Medicine, Washington University School of Medicine, St. Louis, MO

Sara Pajouhanfar

Department of Pediatrics, Division of Genetics and Genomic Medicine, Washington University School of Medicine, St. Louis, MO

Korre Fairman

Department of Pediatrics, Division of Newborn Medicine, Washington University School of Medicine, St. Louis, MO

Catherine Gooch

Department of Pediatrics, Division of Genetics and Genomic Medicine, Washington University School of Medicine, St. Louis, MO