Defective intracellular transport of CLN3 is the molecular basis of Batten disease (JNCL)

Author: Järvelä Irma   Lehtovirta Maarit   Tikkanen Ritva   Kyttälä Aija   Jalanko Anu   Santavuori P.   Mitchison H.M.   Janes R.W.   Munroe P.B.   Lauronen L.   Järvelä I.   Wisniewski K.E.   Järvelä I.   Pearce D.A.   Pearce D.A.   Croopnick J.B.   Fearnley I.M.   Palmer D.N.   Katz M.L.   Zeman W.   Olkkonen V.M.   Williams M.A.   Harter C.   Johnson K.F.   Johnson K.F.   Letourneur F.   Goebel H.H.   Hohman T.C.   Ikonen E.   Riikonen A.   Kyttälä A.   Michalewski M.P.   Linial M.   Ferro-Novick S.   Nixon R.A.   Cameron P.L.   Sanger F.   Andersson S.   Luthman H.   Proia R.L.   Laemmli U.K.   Aniento F.   Tokuyasu K.T.   Slot J.W.   Pohlmann R.   Nakayama Y.  

Publisher: Oxford University Press

ISSN: 1460-2083

Source: Human Molecular Genetics, Vol.8, Iss.6, 1999-06, pp. : 1091-1098

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Abstract