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15 more genetic variants connected to KCNK9 imprinting syndrome are found by researchers.

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The KCNK9 gene contains 15 other genetic abnormalities that result in a neurodevelopmental condition

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according to a multidisciplinary team of researchers lead by the Center for Individualized Medicine at Mayo Clinic. 

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The disorder's symptoms can include intellectual incapacity, behavioural abnormalities,

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speech and movement impairments, and unusual facial traits.

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diagnosis as a result of the new study, which was reported in Genome Medicine.

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The lack of a specific treatment for KCNK9 imprinting syndrome

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Dr. Cousin believes their finding may help in the creation of new medications.

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Always suppressed is the father's gene.