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Results 21-26 of 26 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2002
α-Mannosidosis in the guinea pig: cloning of the lysosomal α-mannosidase cDNA and identification of a missense mutation causing α-mannosidosis
Berg, T.
;
Hopwood, J.
2002
Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome
Lower, K.
;
Turner, G.
;
Kerr, B.
;
Mathews, K.
;
Shaw, M.
;
Gedeon, A.
;
Schelley, S.
;
Hoyme, H.
;
White, S.
;
Delatycki, M.
;
Lampe, A.
;
Clayton-Smith, J.
;
Stewart, H.
;
van Ravenswaay, C.
;
de Vries, B.
;
Cox, B.
;
Grompe, M.
;
Ross, S.
;
Thomas, P.
;
Mulley, J.
;
et al.
2002
Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy
Stromme, P.
;
Mangelsdorf, M.
;
Shaw, M.
;
Lower, K.
;
Lewis, S.
;
Bruyere, H.
;
Lutcherath, V.
;
Gedeon, A.
;
Wallace, R.
;
Scheffer, I.
;
Turner, G.
;
Partington, M.
;
Frints, S.
;
Fryns, J.
;
Sutherland, G.
;
Mulley, J.
;
Gecz, J.
2002
Immune response to enzyme replacement therapy: single epitope control of antigen distribution from circulation
Glaros, E.
;
Turner, C.
;
Parkinson, E.
;
Hopwood, J.
;
Brooks, D.
2002
Role of RegM, a homologue of the catabolite repressor protein CcpA, in the virulence of Streptococcus pneumoniae
Giammarinaro, P.
;
Paton, J.
2002
Complementation of a yeast CYC3 deficiency identifies an X-linked mammalian activator of apocytochrome c
Schwarz, Q.
;
Cox, T.
Discover
Author
3
Bowie, J.
2
Brinkworth, C.
2
et al.
2
Fincher, G.
2
Frints, S.
2
Fryns, J.
2
Gecz, J.
2
Gedeon, A.
2
Hopwood, J.
2
Lower, K.
.
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Subject
25
Molecular Sequence Data
16
Animals
13
Humans
11
Sequence Homology, Amino Acid
8
Mice
7
Base Sequence
6
Binding Sites
6
Mutation
6
Sequence Alignment
5
Cloning, Molecular
.
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