(Q22009467)

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Identification and cloning of putative human neuronal voltage-gated calcium channel gamma-2 and gamma-3 subunits: neurologic implications

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scholarly article

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Identification and cloning of putative human neuronal voltage-gated calcium channel gamma-2 and gamma-3 subunits: neurologic implications (English)

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calcium ion transport

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GOA release 2020-03-11

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author name string

J L Black

1

author given names

J L 3rd

author last names

Black

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PubMed publication ID

7 February 2023

V A Lennon

2

author given names

V A

author last names

Lennon

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PubMed publication ID

7 February 2023

language of work or name

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publication date

April 1999

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74

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4

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357-61

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Absence epilepsy in tottering mutant mice is associated with calcium channel defects

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https://api.crossref.org/works/10.4065%2F74.4.357

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse

1 reference

https://api.crossref.org/works/10.4065%2F74.4.357

7 January 2021

based on heuristic

inferred from DOI database lookup

The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunit.

1 reference

https://api.crossref.org/works/10.4065%2F74.4.357

7 January 2021

based on heuristic

inferred from DOI database lookup

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1 reference

https://api.crossref.org/works/10.4065%2F74.4.357

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based on heuristic

inferred from DOI database lookup

Radicals r'aging

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https://api.crossref.org/works/10.4065%2F74.4.357

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based on heuristic

inferred from DOI database lookup

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

1 reference

https://api.crossref.org/works/10.4065%2F74.4.357

7 January 2021

based on heuristic

inferred from DOI database lookup

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

1 reference

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based on heuristic

inferred from DOI database lookup

Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2

1 reference

https://api.crossref.org/works/10.4065%2F74.4.357

7 January 2021

based on heuristic

inferred from DOI database lookup

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

1 reference

https://api.crossref.org/works/10.4065%2F74.4.357

7 January 2021

based on heuristic

inferred from DOI database lookup

Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16

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based on heuristic

inferred from DOI database lookup

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

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7 January 2021

based on heuristic

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Sequence mapping by electronic PCR

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7 January 2021

based on heuristic

inferred from DOI database lookup

Genome maps 7. The human transcript map. Wall chart

1 reference

https://api.crossref.org/works/10.4065%2F74.4.357

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based on heuristic

inferred from DOI database lookup

A Gene Map of the Human Genome

1 reference

https://api.crossref.org/works/10.4065%2F74.4.357

7 January 2021

based on heuristic

inferred from DOI database lookup

A potassium channel mutation in neonatal human epilepsy

1 reference

https://api.crossref.org/works/10.4065%2F74.4.357

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based on heuristic

inferred from DOI database lookup

Structure and in Vitro Transcription of Human Globin Genes

1 reference

https://api.crossref.org/works/10.4065%2F74.4.357

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based on heuristic

inferred from DOI database lookup

Identifiers

10.4065/74.4.357

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