Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus. (Q45342398)

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29 February 2020

title

Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus (English)

1 reference

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disability affecting intellectual abilities

29 February 2020

main subject

disability

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intellectual disability

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based on heuristic

inferred from title

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6

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29 February 2020

Hadia Hijazi

2

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29 February 2020

Mustafa A. Salih

9

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Tariq Ahmad Masoodi

11

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29 February 2020

Fowzan S Alkuraya

12

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4

Ranad Shaheen

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29 February 2020

author name string

Anas M Alazami

1

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29 February 2020

Mohammed S Al-Dosari

3

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29 February 2020

Amal Hashem

5

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29 February 2020

Jawahir Y Mohamed

7

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29 February 2020

Amal Kentab

8

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29 February 2020

Ali Awaji

10

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language of work or name

English

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publication date

25 April 2013

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Journal of Medical Genetics

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published in

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volume

50

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issue

7

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page(s)

425-430

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The epidemiology of mental retardation: challenges and opportunities in the new millennium

29 February 2020

cites work

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Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

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Deep sequencing reveals 50 novel genes for recessive cognitive disorders

21 January 2018

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easyLINKAGE-Plus--automated linkage analyses using large-scale SNP data

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Interactive visual analysis of SNP data for rapid autozygosity mapping in consanguineous families

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DMLE+: Bayesian linkage disequilibrium gene mapping.

21 January 2018

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An adenosine deaminase that generates inosine at the wobble position of tRNAs

21 January 2018

1 reference

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Compilation of tRNA sequences and sequences of tRNA genes

21 January 2018

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Codon--anticodon pairing: the wobble hypothesis

21 January 2018

1 reference

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Analysis of codon:anticodon interactions within the ribosome provides new insights into codon reading and the genetic code structure

21 January 2018

1 reference

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RNA editing by adenosine deaminases generates RNA and protein diversity

21 January 2018

1 reference

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Mutations in the FTSJ1 gene coding for a novel S-adenosylmethionine-binding protein cause nonsyndromic X-linked mental retardation

21 January 2018

1 reference

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Diagnostic exome sequencing in persons with severe intellectual disability

21 January 2018

1 reference

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10.1136/JMEDGENET-2012-101378

21 January 2018

Identifiers

DOI

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29 February 2020

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