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ain-with-anhidrosis/</loc><lastmod>2026-07-02T00:00:00+00:00</lastmod></url><url><loc>https://biogen.enfermedadesraras.es/homozygous-familial-hypercholesterolemia-experience-with-evinacumab-treatment-in-two-mexican-pediatric-patients-case-report/</loc><lastmod>2026-07-02T00:00:00+00:00</lastmod></url><url><loc>https://biogen.enfermedadesraras.es/case-report-novel-homozygous-pathogenic-variant-of-the-spg20-gene-causes-the-troyer-syndrome-in-china/</loc><lastmod>2026-07-02T00:00:00+00:00</lastmod></url><url><loc>https://biogen.enfermedadesraras.es/epigenetic-cd4-t-cell-quantification-from-dried-blood-spots-using-a-qpcr-based-assay/</loc><lastmod>2026-07-01T22:00:00+00:00</lastmod></url><url><loc>https://biogen.enfermedadesraras.es/segmental-copy-number-variant-detection-using-an-amplicon-based-ngs-panel-for-integrated-glioma-classification/</loc><lastmod>2026-07-01T22:00:00+00:00</lastmod></url><url><loc>https://medicalxpress.com/news/2026-07-results-phase-ii-trial-therapy.html</loc><lastmod>2026-07-01T20:00:09+00:00</lastmod></url><url><loc>https://medicalxpress.com/news/2026-07-gene-diseases-reveals-opposing-dementia.html</loc><lastmod>2026-07-01T16:00:08+00:00</lastmod></url><url><loc>https://medicalxpress.com/news/2026-06-faulty-calcium-dry-mouth-syndrome.html</loc><lastmod>2026-07-01T15:00:21+00:00</lastmod></url><url><loc>https://medicalxpress.com/news/2026-07-rare-muscle-disorder-mutations-reveal.html</loc><lastmod>2026-07-01T15:00:17+00:00</lastmod></url><url><loc>https://biogen.enfermedadesraras.es/icmip-i-as-a-novel-candidate-gene-for-neurodevelopmental-and-neuropsychiatric-disorders/</loc><lastmod>2026-07-01T15:00:00+00:00</lastmod></url><url><loc>https://biogen.enfermedadesraras.es/when-truncation-is-not-loss-of-function-neo-tail-architecture-as-a-determinant-of-pathogenicity-in-nmd-escaping-frameshift-variants/</loc><lastmod>2026-07-01T15:00:00+00:00</lastmod></url><url><loc>https://medicalxpress.com/news/2026-07-national-rare-disease-registry-patients.html</loc><lastmod>2026-07-03T03:00:01+00:00</lastmod></url><url><loc>https://medicalxpress.com/news/2026-07-prostate-cancer-mutations-reveal-responses.html</loc><lastmod>2026-07-02T19:40:03+00:00</lastmod></url><url><loc>https://medicalxpress.com/news/2026-07-genetic-pulmonary-fibrosis-patients.html</loc><lastmod>2026-07-02T18:00:14+00:00</lastmod></url><url><loc>https://biogen.enfermedadesraras.es/longest-surviving-patient-with-a-homozygous-splice-altering-egfr-pathogenic-variant-presenting-with-skin-autoinflammation-and-a-bartter-like-salt-losing-tubulopathy/</loc><lastmod>2026-06-30T16:00:21+00:00</lastmod></url><url><loc>https://biogen.enfermedadesraras.es/functional-characterisation-and-pathological-significance-of-variants-of-mef2c-promoter-in-tetralogy-of-fallot/</loc><lastmod>2026-06-29T16:00:20+00:00</lastmod></url><url><loc>https://biogen.enfermedadesraras.es/care-of-patients-with-phenylketonuria-pku-in-germany-a-claims-data-analysis-from-2013-to-2023/</loc><lastmod>2026-07-02T22:00:00+00:00</lastmod></url><url><loc>https://biogen.enfermedadesraras.es/characterisation-of-the-ismn1-2-i-locus-using-a-highly-specific-variant-caller-on-whole-genome-sequence-data-from-500000-individuals/</loc><lastmod>2026-07-02T15:00:00+00:00</lastmod></url><url><loc>https://biogen.enfermedadesraras.es/real-world-insights-into-neurodevelopmental-outcomes-amongst-people-with-congenital-hyperinsulinism/</loc><lastmod>2026-07-03T22:00:00+00:00</lastmod></url><url><loc>https://biogen.enfermedadesraras.es/correction-follow-up-cancer-risk-and-mortality-in-peutz-jeghers-syndrome-data-from-the-pred-idf-network/</loc><lastmod>2026-07-03T15:00:00+00:00</lastmod></url><url><loc>https://medicalxpress.com/news/2026-07-tumor-high-cell-lymphoma-standard.html</loc><lastmod>2026-07-03T15:00:03+00:00</lastmod></url><url><loc>https://biogen.enfermedadesraras.es/increased-awareness-around-an-ultra-rare-disease-can-improve-diagnosis-delays-the-french-example-in-primary-hyperoxalurias/</loc><lastmod>2026-07-04T22:00:00+00:00</lastmod></url><url><loc>https://biogen.enfermedadesraras.es/patient-driven-surveys-of-mucopolysaccharidoses-revealed-patient-reported-outcomes-in-the-japan-mps-patient-and-family-group/</loc><lastmod>2026-07-03T22:00:00+00:00</lastmod></url><url><loc>https://biogen.enfermedadesraras.es/mapping-the-landscape-of-treatable-inborn-errors-of-metabolism-a-systematic-gene-level-evaluation-based-on-the-icimd-classification/</loc><lastmod>2026-07-03T22:00:00+00:00</lastmod></url><url><loc>https://biogen.enfermedadesraras.es/cognitive-function-in-adult-nf1-patients-without-other-cognitive-disorders-a-cross-sectional-study/</loc><lastmod>2026-07-03T22:00:00+00:00</lastmod></url><url><loc>https://biogen.enfermedadesraras.es/parental-and-public-views-on-genomic-newborn-screening-a-systematic-review/</loc><lastmod>2026-07-04T15:00:00+00:00</lastmod></url><url><loc>https://medicalxpress.com/news/2026-07-survey-europeans-state-funded-fertility.html</loc><lastmod>2026-07-04T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