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on page 1 showing 10 out of 353 results
https://web.expasy.org/cellosaurus/CVCL_EY64

Cite this: (NHCDR Cat# ND30244, RRID:CVCL_EY64)
Organism: Homo sapiens
Disease: Parkinson's disease
Category: Finite cell line
Comment: Sequence variation: Heterozygous for LRRK2 p.Gly2019Ser (c.6055G>A) (NHCDR). Discontinued: Coriell; ND30244.

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https://web.expasy.org/cellosaurus/CVCL_EY91

Cite this: (NHCDR Cat# ND33391, RRID:CVCL_EY91)
Organism: Homo sapiens
Disease:
Category: Finite cell line
Comment: Discontinued: Coriell; ND33391.

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https://web.expasy.org/cellosaurus/CVCL_FA00

Cite this: (NHCDR Cat# ND50004, RRID:CVCL_FA00)
Organism: Homo sapiens
Disease:
Category: Induced pluripotent stem cell
Comment: From: Target ALS Foundation; USA.

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https://web.expasy.org/cellosaurus/CVCL_DD47

Cite this: (NHCDR Cat# ND30171, RRID:CVCL_DD47)
Organism: Homo sapiens
Disease: Parkinson's disease
Category: Finite cell line
Comment: Sequence variation: Heterozygous for PARK2 p.Arg42Pro (c.125G>C) and Ex3del (PubMed=25843045). Discontinued: Coriell; ND30171.

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https://web.expasy.org/cellosaurus/CVCL_DD48

Cite this: (NHCDR Cat# ND29369, RRID:CVCL_DD48)
Organism: Homo sapiens
Disease: Parkinson's disease
Category: Finite cell line
Comment: Sequence variation: Heterozygous for PARK2 p.Arg275Trp (c.823C>T) (Coriell). Discontinued: Coriell; ND29369.

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https://web.expasy.org/cellosaurus/CVCL_DD49

Cite this: (NHCDR Cat# ND31618, RRID:CVCL_DD49)
Organism: Homo sapiens
Disease: Parkinson's disease
Category: Finite cell line
Comment: Sequence variation: Heterozygous for PARK2 p.Arg42Pro (c.125G>C) (Coriell). Discontinued: Coriell; ND31618.

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https://web.expasy.org/cellosaurus/CVCL_DD50

Cite this: (NHCDR Cat# ND29802, RRID:CVCL_DD50)
Organism: Homo sapiens
Disease: Parkinson's disease
Category: Finite cell line
Comment: Sequence variation: LRRK2 p.Gly2019Ser (c.6055G>A) (PubMed=27191603). Discontinued: Coriell; ND29802.

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https://web.expasy.org/cellosaurus/CVCL_DD51

Cite this: (NHCDR Cat# ND29492, RRID:CVCL_DD51)
Organism: Homo sapiens
Disease: Parkinson's disease
Category: Finite cell line
Comment: Sequence variation: Heterozygous for LRRK2 p.Gly2019Ser (c.6055G>A) (PubMed=27191603). Discontinued: Coriell; ND29492.

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https://web.expasy.org/cellosaurus/CVCL_DD53

Cite this: (NHCDR Cat# ND31630, RRID:CVCL_DD53)
Organism: Homo sapiens
Disease: Parkinson's disease
Category: Finite cell line
Comment: Sequence variation: GBA p.Asn409Ser (c.1226A>G) (Coriell). Discontinued: Coriell; ND31630. Discontinued: NHCDR; ND31630.

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https://web.expasy.org/cellosaurus/CVCL_EZ86

Cite this: (NHCDR Cat# ND42717, RRID:CVCL_EZ86)
Organism: Homo sapiens
Disease:
Category: Finite cell line
Comment:

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