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3. O09 Bi-allelic variants of FILIP1 cause congenital myopathy, dysmorphism and neurological defects

7. SMA CLINICAL DATA

8. NEW GENES AND DISEASES

9. Neugeborenenscreening auf spinale Muskelatrophie

11. HEREDITARY NEUROPATHIES & ALS

14. P.211Pilot study of genetic newborn screening for spinal muscular atrophy in Germany: clinical results after more than a year

17. METABOLIC MYOPATHIES II

18. Spinale Muskelatrophie

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