CA8 mutations cause a novel syndrome characterized by ataxia and mild mental retardation with predisposition to quadrupedal gait (Q27312310)

9

0 references

Peter Robinson

10

object named as

Peter N Robinson

0 references

Masoud Garshasbi

object named as

Masoud Garshasbi

3

0 references

author name string

Seval Türkmen

1

0 references

Gao Guo

2

0 references

Katrin Hoffmann

4

0 references

Amjad J Alshalah

5

0 references

Claudia Mischung

6

0 references

Andreas Kuss

7

0 references

Nicholas Humphrey

Creative Commons Attribution 4.0 International

8

0 references

language of work or name

English

0 references

publication date

May 2009

0 references

published in

PLOS Genetics

0 references

volume

5

0 references

issue

5

0 references

page(s)

e1000487

0 references

copyright license

start time

22 May 2009

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

ImageJ

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2677160/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

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Junctional membrane inositol 1,4,5-trisphosphate receptor complex coordinates sensitization of the silent EGF-induced Ca2+ signaling

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Carbonic anhydrase related protein 8 mutation results in aberrant synaptic morphology and excitatory synaptic function in the cerebellum

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