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3 Einträge gefunden

AUNA2: A Novel Type of Non-Syndromic Slowly Progressive Auditory Synaptopathy/Auditory Neuropathy with Autosomal-Dominant Inheritance
2017 - Forschungsinformationssystem des UKE
A TUBB6 mutation is associated with autosomal dominant non-progressive congenital facial palsy, bilateral ptosis and velopharyngeal dysfunction
2017 - Forschungsinformationssystem des UKE
Identification of two novel ALS2 mutations in infantile-onset ascending hereditary spastic paraplegia
2016 - Forschungsinformationssystem des UKE