20 May 2022


NLGN3 Sequencing

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Test Background

Mutations in NLGN3/4 have been associated with autism spectrum disorders and mental retardation. NLGN3/4 is inherited in an X-linked manner.

This laboratory performs Sanger sequencing of the NLGN3 gene.

Gene(s)

NLGN3

Useful Links

About Claritas

Claritas Genomics serves children affected with complex genetic disorders by providing timely and accurate results, resolving families’ long search for answers. By combining clinical expertise of the world’s best pediatric specialists with innovative platform solutions, Claritas is working to improve patient care and enable new discoveries. We are committed to the highest quality and accessibility of information and our interpretive services and unique approach to reporting set the standard for reliably and clearly communicating genetic information.

Now is the time to integrate genomics into clinical practice to inform, guide and improve medical treatment for kids around the world.


 
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