A novel mutation in L1CAM causes a mild form of L1 syndrome: a case report.
Maarten OtterMarijke WeversMarline PistersRolph PfundtYvonne VosRutger Jan NievelsteinConstance StumpelPublished in: Clinical case reports (2017)
Clinical geneticists, neurologists, psychiatrists, and other healthcare providers can learn from this case report that patients with a behavioral phenotype that includes a mild learning disability may also require a thorough examination, including brain MRI and whole-exome sequencing.