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Article

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

Acta neurologica Belgica - 1 Jun 2016

Samanta Debopam

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Share to Agenesis of Corpus Callosum
Share to Developmental Disabilities
Share to SOS1 gene
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 26280111
DOI: 10.1007/s13760-015-0526-9

Genes

SOS1

Provenance

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Severe developmental delay and complete agenesis of corpus callosum in a Noonan syndrome patient with SOS1 mutation.PMID 26280111Read ↗

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