(Q43268814)

17 November 2017

title

A novel mutation in the DLG3 gene encoding the synapse-associated protein 102 (SAP102) causes non-syndromic mental retardation (English)

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17 November 2017

9

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17 November 2017

Ginevra Zanni

1

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Karine Poirier

object named as

Karine Poirier

5

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author name string

Hilde van Esch

2

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17 November 2017

Anissa Bensalem

3

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17 November 2017

Yoann Saillour

4

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17 November 2017

Laetitia Castelnau

6

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17 November 2017

Hans Hilger Ropers

7

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17 November 2017

Arjan P M de Brouwer

8

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17 November 2017

Jean-Pierre Fryns

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Jamel Chelly

11

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17 November 2017

publication date

1 October 2009

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17 November 2017

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17 November 2017

volume

11

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17 November 2017

issue

2

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17 November 2017

page(s)

251-255

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https://scigraph.springernature.com/pub.10.1007/s10048-009-0224-y

17 November 2017

exact match

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cites work

Synaptic trafficking of glutamate receptors by MAGUK scaffolding proteins

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12 December 2020

Fragile X syndrome: loss of local mRNA regulation alters synaptic development and function

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12 December 2020

Decreased NR1, NR2A, and SAP102 transcript expression in the hippocampus in bipolar disorder

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12 December 2020

Differential trafficking of AMPA and NMDA receptors by SAP102 and PSD-95 underlies synapse development

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12 December 2020

Genetics and pathophysiology of mental retardation

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12 December 2020

Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation

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12 December 2020

Loss of X-linked mental retardation gene oligophrenin1 in mice impairs spatial memory and leads to ventricular enlargement and dendritic spine immaturity.

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12 December 2020

The mental retardation protein PAK3 contributes to synapse formation and plasticity in hippocampus

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12 December 2020

Monogenic X-linked mental retardation: is it as frequent as currently estimated? The paradox of the ARX (Aristaless X) mutations.

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12 December 2020

Mutation frequencies of X-linked mental retardation genes in families from the EuroMRX consortium.

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12 December 2020

Synapse-associated protein 102/dlgh3 couples the NMDA receptor to specific plasticity pathways and learning strategies.

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12 December 2020

Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation

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12 December 2020

NMDA receptor trafficking in synaptic plasticity and neuropsychiatric disorders

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12 December 2020

Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation

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12 December 2020

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12 December 2020

X-linked mental retardation: focus on synaptic function and plasticity.

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12 December 2020

Denaturing high-performance liquid chromatography using the WAVE DNA fragment analysis system

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12 December 2020

A developmental change in NMDA receptor-associated proteins at hippocampal synapses

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12 December 2020

PDZ domain proteins of synapses

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12 December 2020

The role of neuronal complexes in human X-linked brain diseases

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12 December 2020

10.1007/S10048-009-0224-Y

Identifiers

DOI

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17 November 2017

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