-
disability syndrome. Eur J Med
Genet 57(10):543-551
Rahikkala E,
Myllykoski M,
Hinttala R,
Vieira P,
Nayebzadeh N,
Weiss S,
Plomp A,
Bittner RE,
Kurki MI, Kuismin...
- Henna; Vieira, Päivi; Zarybnicky, Tomas; Sipilä, Petra; Kuure, Satu;
Hinttala,
Reetta (2022-10-01). "The
Finnish genetic heritage in 2022 – from diagnosis...
- 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
Kervinen M,
Hinttala R,
Helander HM, et al. (2006). "The
MELAS mutations 3946 and 3949 perturb...