CLN6, which is associated with a lysosomal storage disease, is an endoplasmic reticulum protein (Q24299818)

lysosomal storage disease

GOA release 2020-03-11

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Gregoire Michaux

2

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Daniel F Cutler

object named as

Daniel F Cutler

6

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Sara E. Mole

object named as

Sara E Mole

1

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author name string

Sandra Codlin

3

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Ruth B Wheeler

4

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Julie D Sharp

Experimental Cell Research

5

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language of work or name

English

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publication date

15 August 2004

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published in

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volume

298

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issue

2

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page(s)

399-406

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cites work

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Defective intracellular transport of CLN3 is the molecular basis of Batten disease (JNCL)

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The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8

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The gene mutated in variant late-infantile neuronal ceroid lipofuscinosis (CLN6) and in nclf mutant mice encodes a novel predicted transmembrane protein

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inferred from DOI database lookup

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based on heuristic

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