7 results on '"Fialho D"'
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2. A new explanation for recessive myotonia congenita: Exon deletions and duplications in CLCN1
3. Clinical and Molecular Characterization of Non-Dystrophic Myotonia (P05.181)
4. EEG Abnormalities in the Episodic Ataxias (P05.029)
5. What causes paramyotonia in the United Kingdom?: Common and new SCN4A mutations revealed
6. POLG1 , C10ORF2 , and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletions
7. Andersen–Tawil syndrome
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