464 resources

Cell Lines SCA3

Pa2-SCA3

Cell type
hiPSC
Causal gene(s)
ATXN3
Mutation
78 CAG
Originating lab
Chinese Academy of Sciences
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Cell Lines SPG7

Patient 1

Cell type
hiPSC
Causal gene(s)
SPG7
Mutation
c.1449 + 1G > A (exon 10) and c.1529C>T (exon 11)
Originating lab
University of Sydney
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Cell Lines MSA/OPCA

Patient 1 (MSA-P)

Cell type
Fibroblast
Causal gene(s)
GGC expansion in NOTCH2NLC
Mutation
112-138 GGC
Originating lab
First Affiliated Hospital of Nanchang University
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Cell Lines SPG7

Patient 2

Cell type
hiPSC
Causal gene(s)
SPG7
Mutation
c.415C > T (exon 4) and c.941T>A (exon 7)
Originating lab
University of Sydney
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Cell Lines SPG7

Patient 3

Cell type
hiPSC
Causal gene(s)
SPG7
Mutation
chr16:g.89623293A > G, c.2182-2A > G (intron 16- exon 17) and c.1529C>T (exon 11)
Originating lab
University of Sydney
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Cell Lines MSA/OPCA

Patient 4 (MSA-C)

Cell type
Fibroblast
Causal gene(s)
GGC expansion in NOTCH2NLC
Mutation
101-126 GGC
Originating lab
First Affiliated Hospital of Nanchang University
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Cell Lines SACS/ARSACS/SPAX6

Patient line 1

Cell type
Fibroblast
Causal gene(s)
SACS
Mutation
c.8339T>C (p.Phe2780Cys) and c.12416T>C (p.Leu4139Ser)/c.11675C>G (p.Ser3892X) (sibling from patient line 2)
Originating lab
UCL Queen Square Institute of Neurology
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Cell Lines SACS/ARSACS/SPAX6

Patient line 2

Cell type
Fibroblast
Causal gene(s)
SACS
Mutation
c.8339T>C (p.Phe2780Cys) and c.12416T>C (p.Leu4139Ser)/c.11675C>G (p.Ser3892X) (sibling from patient line 1)
Originating lab
UCL Queen Square Institute of Neurology
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Twenty Twenty-Five

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