PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndrome

  1. Donaldson, M.R.
  2. Jensen, J.L.
  3. Tristani-Firouzi, M.
  4. Tawil, R.
  5. Bendahhou, S.
  6. Suarez, W.A.
  7. Cobo, A.M.
  8. Poza, J.J.
  9. Behr, E.
  10. Wagstaff, J.
  11. Szepetowski, P.
  12. Pereira, S.
  13. Mozaffar, T.
  14. Escolar, D.M.
  15. Fu, Y.-H.
  16. Ptácek, L.J.
Aldizkaria:
Neurology

ISSN: 0028-3878

Argitalpen urtea: 2003

Alea: 60

Zenbakia: 11

Orrialdeak: 1811-1816

Mota: Artikulua

DOI: 10.1212/01.WNL.0000072261.14060.47 GOOGLE SCHOLAR

Garapen Iraunkorreko Helburuak