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Your search keyword '"Başak, Ayşe Nazlı (ORCID 0000-0001-9257-3540 ' showing total 7 results

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7 results on '"Başak, Ayşe Nazlı (ORCID 0000-0001-9257-3540 '

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1. Human CRY1 variants associate with attention deficit/hyperactivity disorder

2. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

3. Bi-allelic variants in HOPS complex subunit VPS41 cause cerebellar ataxia and abnormal membrane trafficking

4. Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis

5. Natural History, Phenotypic Spectrum, and Discriminative Features of Multisystemic RFC1 Disease

6. The effect of SMN gene dosage on ALS risk and disease severity

7. Clinico-Genetic, Imaging and Molecular Delineation of COQ8A-Ataxia: A Multicenter Study of 59 Patients

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