Department of Medical Genetics

Organisational unit: Institution

Latest publications

  1. CHCHD10 mutations are not a common cause of SMN1-negative type III/IV spinal motor atrophy Reply

    Publication: Contribution to journalB1 Unrefereed journal article

  2. Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family

    Publication: Contribution to journalA1 Refereed journal article

Research publications per year

No data available

ID: 1469