MUTATIONS IN HYAL2, ENCODING HYALURONIDASE 2, CAUSE A SYNDROME OF OROFACIAL CLEFTING AND COR TRIATRIATUM SINISTER IN HUMANS AND MICE.

Mutations in HYAL2, Encoding Hyaluronidase 2, Cause a Syndrome of Orofacial Clefting and Cor Triatriatum Sinister in Humans and Mice.

Orofacial clefting is amongst the most common of birth defects, with both genetic and environmental components.Although numerous studies have been undertaken to investigate the complexities of the genetic etiology of this heterogeneous condition, this factor remains incompletely understood.Here, we describe mutations in the HYAL2 gene as a cause of

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Semantic Interoperability for IoT Platforms in Support of Decision Making: An Experiment on Early Wildfire Detection

One of the main obstacles towards the promotion of IoT adoption and innovation is data interoperability.Facilitating cross-domain interoperability is expected to be the core element for the realisation of the next generation of the IoT computing paradigm that is already Grains taking shape under the name of Internet of Everything (IoE).In this arti

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