Deciphering the genetic link between familial hypobetalipoproteinemia and neuromuscular disorder: a case report
{{output}}
Background: We present a case of a white 21-year-old male patient who showed symptoms of both Familial hypobetalipoproteinemia and neuromuscular abnormalities linked to a mutation (c.7564C > T) in the APOB gene in addition to sev... ...
