Varaico: Literature-Extracted Genetic Variants

Gene:PRKAR1B
Variant:p.E196K
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PRKAR1B

NM_001164760.2:p.E196K

Associated Papers

Expansion of the Phenotypic and Genotypic Spectrum for PRKAR1B-Related Marbach-Schaaf Neurodevelopmental Syndrome: A Case Series.

Burkart S et al.

Clinical Genetics, 2025

Protein Kinase A in neurological disorders.

Glebov-McCloud AGP et al.

Journal of Neurodevelopmental Disorders, 2024

Phenotypic characterization of seven individuals with Marbach-Schaaf neurodevelopmental syndrome.

Marbach F et al.

American Journal of Medical Genetics. Part A, 2022

Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain.

Marbach F et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."