Detection of biotinidase gene mutations in Turkish patients ascertained by newborn and family screening

Yerel katalogda bu makaleye atıf yapan 42 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).

1. 2020 Biotinidase Deficiency: Prevalence, Impact And Management StrategiesAtıf 90 · OpenAlex
2. 2017 A treatable cause of myelopathy and vision loss mimicking neuromyelitis optica spectrum disorder: late-onset biotinidase deficiencyAtıf 38 · OpenAlex
3. 2017 A treatable cause of myelopathy and vision loss mimicking neuromyelitis optica spectrum disorder: Late-onset biotinidase deficiencyAtıf 38 · OpenAlex
4. 2017 A treatable cause of myelopathy and vision loss mimicking neuromyelitis optica spectrum disorder: late-onset biotinidase deficiencyAtıf 38 · OpenAlex
5. 2017 A treatable cause of myelopathy and vision loss mimicking neuromyelitis optica spectrum disorder: late-onset biotinidase deficiencyAtıf 38 · OpenAlex
6. 2018 Single center experience of biotinidase deficiency: 259 patients and six novel mutationsAtıf 37 · OpenAlex
7. 2018 Single center experience of biotinidase deficiency: 259 patients and six novel mutationsAtıf 37 · OpenAlex
8. 2018 Single center experience of biotinidase deficiency: 259 patients and six novel mutationsAtıf 37 · OpenAlex
9. 2018 Single center experience of biotinidase deficiency: 259 patients and six novel mutationsAtıf 37 · OpenAlex
10. 2018 Single center experience of biotinidase deficiency: 259 patients and six novel mutationsAtıf 37 · OpenAlex