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You searched for: Author/Creator Voermans, Nicol C.

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2. A novel role for the extracellular matrix glycoprotein‐Tenascin‐X in gastric function. (23rd January 2019)

3. Aberrant regulation of epigenetic modifiers contributes to the pathogenesis in patients with selenoprotein N‐related myopathies. Issue 7 (1st April 2019)

6. Biallelic loss of function variants in SYT2 cause a treatable congenital onset presynaptic myasthenic syndrome. Issue 10 (10th August 2020)

8. Clinical, genetic, and histological features of centronuclear myopathy in the Netherlands. Issue 6 (25th September 2021)

10. Dejerine–Sottas disease in childhood—Genetic and sonographic heterogeneity. Issue 4 (21st February 2018)