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A novel mutation in L1CAM causes a mild form of L1 syndrome: a case report.

Maarten OtterMarijke WeversMarline PistersRolph PfundtYvonne VosRutger Jan NievelsteinConstance Stumpel
Published 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.
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