Publications
Export 3 results:
Author Title [ Year
] Filters: Author is Çağlayan, Ahmet Okay and Keyword is Adolescent [Clear All Filters]
Brain malformations associated with Knobloch syndrome--review of literature, expanding clinical spectrum, and identification of novel mutations. Pediatr Neurol 51, 806-813.e8 (2014).
NGLY1 mutation causes neuromotor impairment, intellectual disability, and neuropathy. Eur J Med Genet 58, 39-43 (2015).
