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Publications by Maria Ravanini
A Hypomorphic R229Q Rag2 Mouse Mutant Recapitulates Human Omenn Syndrome
Journal of Clinical Investigation
Medicine
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Analysis of Mutations From SCID and Omenn Syndrome Patients Reveals the Central Role of the Rag2 PHD Domain in Regulating V(D)J Recombination
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First Reported Case of Omenn Syndrome in a Patient With Reticular Dysgenesis
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AIRE Deficiency in Thymus of 2 Patients With Omenn Syndrome
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Incomplete X-Inactivation Initiated by a Hypomorphic Xist Allele in the Mouse
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Zic2 Hypomorphic Mutant Mice as a Schizophrenia Model and ZIC2 Mutations Identified in Schizophrenia Patients
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Characterization of a Mouse Model of Obesity-Related Fibrotic Cardiomyopathy That Recapitulates Features of Human Heart Failure With Preserved Ejection Fraction
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