Ara
Toplam kayıt 13, listelenen: 11-13
An interesting case: 30-year-old male patient with myotonic dystrophy typeI has got normal CTG repeats sequence in the DMPK gene, but it does not comply with its clinical features
(SPRINGERNATURE, 2020)
No Abstract Available
A family with mutation in DMD that inherited from gonadal mosaic mother
(SPRINGERNATURE, 2022)
No Abstract Available
CLINICAL COURSE OF ADOLESCENT ONSET ATYPICAL HEMOLYTIC UREMIC SYNDROME: A STUDY OF TURKISH AHUS REGISTRY
(Springer, 2022)
No Abstract Available