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Results 1-6 of 6 (Search time: 0.001 seconds).
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Issue Date
Title
Author(s)
1995
The molecular genetics of mucopolysaccharidosis type I : Diagnostic, clinical and biological implications
Scott, H.
;
Bunge, S.
;
Gal, A.
;
Clarke, L.
;
Morris, C.
;
Hopwood, J.
2004
Twenty-two novel mutations in the lysosomal a-glucosidase gene (GAA) underscore the genotype-phenotype correlation in glycogen storage disease type II
Hermans, M.
;
van Leenen, D.
;
Kroos, M.
;
Beesley, C.
;
Van der Ploeg, A.
;
Sakuraba, H.
;
Wevers, R.
;
Kleijer, W.
;
Mikelakakis, H.
;
Kirk, E.
;
Fletcher, J.
;
Bosshard, N.
;
Basel-Vanagaite, L.
;
Besley, G.
;
Reuser, A.
2002
Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARX
Stromme, P.
;
Mangelsdorf, M.
;
Scheffer, I.
;
Gecz, J.
2005
Neonatal epilepsy syndromes and generalized epilepsy with febrile seizures plus (GEFS+)
Scheffer, I.
;
Harkin, L.
;
Dibbens, L.
;
Mulley, J.
;
Berkovic, S.
2002
Generalized epilepsy with febrile seizures plus: Mutation of the sodium channel subunit SCN1B
Wallace, R.
;
Scheffer, I.
;
Parasivam, G.
;
Barnett, S.
;
Wallace, G.
;
Sutherland, G.
;
Berkovic, S.
;
Mulley, J.
2001
Prediction of Sanfilippo phenotype severity from immunoquantification of heparan-N-sulfamidase in cultured fibroblasts from mucopolysaccharidosis type IIIA patients
Perkins, K.
;
Muller, V.
;
Weber, B.
;
Hopwood, J.
Discover
Author
3
Scheffer, I.
2
Berkovic, S.
2
Hopwood, J.
2
Mulley, J.
1
Barnett, S.
1
Basel-Vanagaite, L.
1
Beesley, C.
1
Besley, G.
1
Bosshard, N.
1
Bunge, S.
.
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Subject
6
Humans
4
Child, Preschool
3
Male
2
Adolescent
2
Child
2
Epilepsies, Myoclonic
2
Epilepsy, Generalized
2
Female
2
Genotype
2
Infant, Newborn
.
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Date issued
1
2005
1
2004
2
2002
1
2001
1
1995