Associated Papers
Two pathogenic NF1 gene mutations identified in DNA from a child with mild phenotype.
Terzi YK et al.
Child's Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery, 2012
Absence of exon 17 c.2970-2872delAAT mutation in Turkish NF1 patients with mild phenotype.
Terzi YK et al.
Child's Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery, 2011
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