The FVB-nmd SMARD1 mouse presents with early respiratory deficits and pathology that significantly impact lifespan
{{output}}
Spinal muscular atrophy with respiratory distress type 1 (SMARD1) is a rare, inherited genetic disease caused by mutations in the immunoglobulin mu binding protein (IGHMBP2) gene that result in spinal muscular atrophy with respiratory distress (SMARD1) or Char... ...
