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Results:
1-7
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Results: 7
Authors:
Leung, KY
Greene, NDE
Munroe, PB
Mole, SE
Citation: Ky. Leung et al., Identification of a transactivation motif in the CLN3 protein, IUBMB LIFE, 51(5), 2001, pp. 295-298
Authors:
Munroe, PB
Caulfield, MJ
Citation: Pb. Munroe et Mj. Caulfield, Genetics of hypertension, CUR OP GEN, 10(3), 2000, pp. 325-329
Authors:
Stephenson, JBP
Greene, NDE
Leung, KY
Munroe, PB
Mole, SE
Gardiner, RM
Taschner, PEM
O'Regan, M
Naismith, K
Crow, YJ
Mitchison, HM
Citation: Jbp. Stephenson et al., The molecular basis of GROD-storing neuronal ceroid lipofuscinoses in Scotland, MOL GEN MET, 66(4), 1999, pp. 245-247
Authors:
Munroe, PB
Olgunturk, RO
Fryns, JP
Van Maldergem, L
Ziereisen, F
Yuksel, B
Gardiner, RM
Chung, E
Citation: Pb. Munroe et al., Mutations in the gene encoding the human matrix Gla protein cause Keutel syndrome, NAT GENET, 21(1), 1999, pp. 142-144
Authors:
Mole, SE
Mitchison, HM
Munroe, PB
Citation: Se. Mole et al., Molecular basis of the neuronal ceroid lipofuscinoses: Mutations in CLN1, CLN2, CLN3, and CLN5, HUM MUTAT, 14(3), 1999, pp. 199-215
Authors:
Hofman, I
Kohlschutter, A
Santavuori, P
Gottlob, I
Goebel, HH
Lake, BD
Schutgens, RBH
Greene, NDE
Leung, KY
Mitchison, HM
Munroe, PB
Taschner, PEM
Citation: I. Hofman et al., Juvenile NCL, BIOM HLTH R, 33, 1999, pp. 55-76
Authors:
Lauronen, L
Munroe, PB
Jarvela, I
Autti, T
Mitchison, HM
O'Rawe, AM
Gardiner, RM
Mole, SE
Puranen, J
Hakkinen, AM
Kirveskari, E
Santavuori, P
Citation: L. Lauronen et al., Delayed classic and protracted phenotypes of compound heterozygous juvenile neuronal ceroid lipofuscinosis, NEUROLOGY, 52(2), 1999, pp. 360-365
Risultati:
1-7
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