(Q48367536)

English

Mutation screening of the KCNN3 gene reveals a rare frameshift mutation

scientific article published in May 2001

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1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

Mutation screening of the KCNN3 gene reveals a rare frameshift mutation (English)

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

Bastiaan Hoogendoorn

9

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

10

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

Geraldine McCarthy

14

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

Michael C O'Donovan

19

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

author name string

T Bowen

1

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

N Williams

2

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

N Norton

3

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

G Spurlock

4

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

O H Wittekindt

5

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

D J Morris-Rosendahl

6

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

H Williams

7

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

L Brzustowicz

8

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

G Jones

11

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

R D Sanders

12

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

L A Jones

13

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

S Jones

15

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

A Bassett

16

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

A G Cardno

17

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

M J Owen

18

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Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

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publication date

1 May 2001

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Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

Molecular Psychiatry

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Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

6

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Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

3

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Europe PubMed Central

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11 February 2018

http://europepmc.org/abstract/MED/11326292

259-260

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Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

Isolation of a novel potassium channel gene hSKCa3 containing a polymorphic CAG repeat: a candidate for schizophrenia and bipolar disorder?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000128

7 January 2021

based on heuristic

inferred from DOI database lookup

Candidate-gene association studies of schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000128

7 January 2021

based on heuristic

inferred from DOI database lookup

Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000128

7 January 2021

based on heuristic

inferred from DOI database lookup

The human small conductance calcium-regulated potassium channel gene (hSKCa3) contains two CAG repeats in exon 1, is on chromosome 1q21.3, and shows a possible association with schizophrenia.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000128

7 January 2021

based on heuristic

inferred from DOI database lookup

A piece in the puzzle: an ion channel candidate gene for schizophrenia.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000128

7 January 2021

based on heuristic

inferred from DOI database lookup

Comparative sequencing of the proneurotensin gene and association studies in schizophrenia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4000128

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.MP.4000128

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/11326292

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