(Q28205749)

1

Heidi C Howard

0 references

Michael P. McDonald

Michael P McDonald

20

0 references

Jean-Pierre Bouchard

21

Jean-Pierre Bouchard

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Jean Mathieu

22

Jean Mathieu

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Nicolas Dupré

5

Nicolas Dupré

0 references

Eric Delpire

23

Eric Delpire

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Daniel Rochefort

3

Daniel Rochefort

0 references

Jean-Baptiste Rivière

9

Jean-Baptiste Rivière

0 references

author name string

David B Mount

2

0 references

Nellie Byun

4

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Jianming Lu

6

0 references

Xuemo Fan

7

0 references

Luyan Song

8

0 references

Claude Prévost

10

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Jürgen Horst

11

0 references

Alessandro Simonati

12

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Beate Lemcke

13

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Rick Welch

14

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Roger England

15

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Frank Q Zhan

16

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Adriana Mercado

17

0 references

William B Siesser

18

0 references

Alfred L George

Corpus Callosum Agenesis and Psychosis in Andermann Syndrome

19

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language of work or name

English

0 references

publication date

November 2002

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published in

Nature Genetics

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volume

32

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page(s)

384-92

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issue

3

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cites work

1 reference

Occurrence of Andermann syndrome out of French Canada--agenesis of the corpus callosum with neuronopathy.

21 January 2018

1 reference

Familial progressive sensorimotor neuropathy with agenesis of the corpus callosum (Andermann syndrome): a clinical, neuroradiological and histopathological study

21 January 2018

1 reference

Fine mapping the candidate region for peripheral neuropathy with or without agenesis of the corpus callosum in the French Canadian population.

21 January 2018

1 reference

Cloning and characterization of KCC3 and KCC4, new members of the cation-chloride cotransporter gene family

21 January 2018

1 reference

Cloning, characterization, and chromosomal location of a novel human K+-Cl- cotransporter

21 January 2018

1 reference

Human and murine phenotypes associated with defects in cation-chloride cotransport

21 January 2018

1 reference

Localization of the K(+)-Cl(-) cotransporter, KCC3, in the central and peripheral nervous systems: expression in the choroid plexus, large neurons and white matter tracts

21 January 2018

1 reference

A dominant negative mutant of the KCC1 K-Cl cotransporter: both N- and C-terminal cytoplasmic domains are required for K-Cl cotransport activity.

21 January 2018

1 reference

The structural unit of the secretory Na+-K+-2Cl- cotransporter (NKCC1) is a homodimer

21 January 2018

1 reference

Functional and molecular characterization of the K-Cl cotransporter of Xenopus laevis oocytes

21 January 2018

1 reference

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

21 January 2018

1 reference

Human diseases: clues to cracking the connexin code?

21 January 2018

1 reference

The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy

21 January 2018

1 reference

Human genetics: lessons from Quebec populations

21 January 2018

1 reference

Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption

21 January 2018

1 reference

Dependence of KCC2 K-Cl cotransporter activity on a conserved carboxy terminus tyrosine residue

21 January 2018

1 reference

Genetic background changes the pattern of forebrain commissure defects in transgenic mice underexpressing the beta-amyloid-precursor protein

21 January 2018

1 reference

Human studies of prepulse inhibition of startle: normal subjects, patient groups, and pharmacological studies

21 January 2018

1 reference

Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus

21 January 2018

1 reference

K-Cl cotransport: properties and molecular mechanism

21 January 2018

1 reference

The KCl cotransporter isoform KCC3 can play an important role in cell growth regulation

21 January 2018

1 reference

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

21 January 2018

1 reference

Dicistronic targeting constructs: reporters and modifiers of mammalian gene expression.

21 January 2018

1 reference

Mouse model of GM2 activator deficiency manifests cerebellar pathology and motor impairment

21 January 2018

1 reference

Bone marrow transplantation prolongs life span and ameliorates neurologic manifestations in Sandhoff disease mice

21 January 2018

1 reference

Social interaction and sensorimotor gating abnormalities in mice lacking Dvl1

21 January 2018

1 reference

Genetic epidemiology of sensorimotor polyneuropathy with or without agenesis of the corpus callosum in northeastern Quebec

21 January 2018

1 reference

Occurrence of Andermann syndrome out of French Canada--agenesis of the corpus callosum with neuronopathy

21 January 2018

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Biochemical and morphometric analyses show that myelination in the insulin-like growth factor 1 null brain is proportionate to its neuronal composition.

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NG1002

1 reference

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

1728585

1033680191

0 references

1728585

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference