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Severe developmental delay and complete agenesis of corpus callosum in a Noonan syndrome patient with SOS1 mutation

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References

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The authors received no financial support for the research, authorship, and/or publication of this article.

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  1. Division of Child Neurology, University of Arkansas for Medical Sciences, 1 Children’s Way, Little Rock, AR, 72202, USA

    Debopam Samanta

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  1. Debopam Samanta
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Correspondence to Debopam Samanta.

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Samanta, D. Severe developmental delay and complete agenesis of corpus callosum in a Noonan syndrome patient with SOS1 mutation. Acta Neurol Belg 116, 223–224 (2016). https://doi.org/10.1007/s13760-015-0526-9

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  • DOI: https://doi.org/10.1007/s13760-015-0526-9

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