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Identification of novel genetic causes of Rett syndrome-like phenotypes | Synapse

January 6, 2016Open Access

Identification of novel genetic causes of Rett syndrome-like phenotypes

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Resumen

Network analysis reveals that these genes interact by means of protein interactions with each other and with the known RTT genes. These findings expand the phenotypical spectrum of previously known NDD genes to encompass RTT-like clinical presentations and identify new candidate genes for RTT-like phenotypes.

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Cite This Study

Lopes et al. (Wed,) studied this question.

synapsesocial.com/papers/69de96e25e582bd3c5e93a16 https://doi.org/https://doi.org/10.1136/jmedgenet-2015-103568

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