(Q33725846)

English

Exome sequencing identifies de novo gain of function missense mutation in KCND2 in identical twins with autism and seizures that slows potassium channel inactivation

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scholarly article

1 reference

Europe PubMed Central

28 July 2017

Exome sequencing identifies de novo gain of function missense mutation in KCND2 in identical twins with autism and seizures that slows potassium channel inactivation (English)

1 reference

Europe PubMed Central

28 July 2017

0 references

Harley I Kornblum

3

object named as

Harley I Kornblum

1 reference

Europe PubMed Central

28 July 2017

Stanley F Nelson

5

object named as

Stanley F Nelson

1 reference

Europe PubMed Central

28 July 2017

author name string

Hane Lee

1

1 reference

Europe PubMed Central

28 July 2017

Meng-chin A Lin

2

1 reference

Europe PubMed Central

28 July 2017

Diane M Papazian

4

1 reference

Europe PubMed Central

28 July 2017

publication date

5 February 2014

1 reference

Europe PubMed Central

28 July 2017

Human Molecular Genetics

1 reference

Europe PubMed Central

28 July 2017

23

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Europe PubMed Central

28 July 2017

13

1 reference

Europe PubMed Central

28 July 2017

3481-3489

1 reference

Europe PubMed Central

28 July 2017

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1 reference

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Structural variation of chromosomes in autism spectrum disorder

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Structural basis for modulation of Kv4 K+ channels by auxiliary KChIP subunits

1 reference

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Multiprotein assembly of Kv4.2, KChIP3 and DPP10 produces ternary channel complexes with ISA-like properties

1 reference

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Intracellular gate opening in Shaker K+ channels defined by high-affinity metal bridges.

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12 December 2020

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Identifiers

10.1093/HMG/DDU056

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

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