All individuals with variants in gene RIPPLY2

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00410556 Pat18 PubMed: Schuermans 2022 analysis 329 adult patients suffering from undiagnosed rare disease; 2-generation family, 1 affected, unaffected heterozygous carrier parents F yes Belgium Tunisia - - - - ? see paper; ..., onset neonatal, disabling chronic migraine, torticollis, cervical vertebral fusions; MRI brain widened Virchow-Robin spaces, periventricular white matter hyperintensities; no family history 1 1 Johan den Dunnen
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