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2. A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy. Issue 1 (December 2016)

3. Abstracts from the 3rd International Genomic Medicine Conference (3rd IGMC 2015). (July 2016)

6. Clinical and biochemical features associated with BCS1L mutation. Issue 5 (19th September 2012)

7. Clinico‐radiological features, molecular spectrum, and identification of prognostic factors in developmental and epileptic encephalopathy due to inosine triphosphate pyrophosphatase (ITPase) deficiency. Issue 3 (12th January 2022)

8. Deletion of low molecular weight protein tyrosine phosphatase (Acp1) protects against stress‐induced cardiomyopathy. Issue 4 (1st September 2015)