Whole exome sequencing identifies a splicing mutation in NSUN2 as a cause of a Dubowitz-like syndrome

  1. Martinez, F.J.
  2. Lee, J.H.
  3. Lee, J.E.
  4. Blanco, S.
  5. Nickerson, E.
  6. Gabrie, S.
  7. Frye, M.
  8. Al-Gazali, L.
  9. Gleeson, J.G.
Aldizkaria:
Journal of Medical Genetics

ISSN: 0022-2593 1468-6244

Argitalpen urtea: 2012

Alea: 49

Zenbakia: 6

Orrialdeak: 380-385

Mota: Artikulua

DOI: 10.1136/JMEDGENET-2011-100686 GOOGLE SCHOLAR

Garapen Iraunkorreko Helburuak