LETM1, a gene deleted in Wolf-Hirschhorn syndrome, encodes an evolutionarily conserved mitochondrial protein (Q33974957)

30 July 2017

title

LETM1, a gene deleted in Wolf-Hirschhorn syndrome, encodes an evolutionarily conserved mitochondrial protein (English)

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30 July 2017

main subject

Wolf-Hirschhorn syndrome

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Stephanie Schlickum

1

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30 July 2017

Abhay Moghekar

2

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Jeremy C Simpson

3

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Cordula Steglich

4

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Richard J O'Brien

5

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Andreas Winterpacht

6

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Sabine U Endele

7

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publication date

1 February 2004

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30 July 2017

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volume

83

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issue

2

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page(s)

254-261

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A transcript map of the newly defined 165 kb Wolf-Hirschhorn syndrome critical region

30 July 2017

cites work

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.013

WHSC1, a 90 kb SET domain-containing gene, expressed in early development and homologous to a Drosophila dysmorphy gene maps in the Wolf-Hirschhorn syndrome critical region and is fused to IgH in t(4;14) multiple myeloma

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.013

Comparative analysis of a novel gene from the Wolf-Hirschhorn/Pitt-Rogers-Danks syndrome critical region

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.013

LETM1, a novel gene encoding a putative EF-hand Ca(2+)-binding protein, flanks the Wolf-Hirschhorn syndrome (WHS) critical region and is deleted in most WHS patients

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.013

First known microdeletion within the Wolf-Hirschhorn syndrome critical region refines genotype-phenotype correlation

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.013

Mapping the Wolf-Hirschhorn syndrome phenotype outside the currently accepted WHS critical region and defining a new critical region, WHSCR-2.

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.013

Genetic basis of mitochondrial function and morphology in Saccharomyces cerevisiae

7 January 2021

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Skeletal muscle mitochondrial defects in nonspecific neurologic disorders.

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.013

Mitochondrial biogenesis defects and neuromuscular disorders

7 January 2021

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Mitochondrial diseases in man and mouse

7 January 2021

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The role of mitochondria in epileptogenesis

7 January 2021

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Neuronal degeneration and mitochondrial dysfunction

7 January 2021

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CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

7 January 2021

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SAP - a putative DNA-binding motif involved in chromosomal organization

7 January 2021

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SAF-Box, a conserved protein domain that specifically recognizes scaffold attachment region DNA.

7 January 2021

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A multitude of suppressors of group II intron-splicing defects in yeast

7 January 2021

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Identification of nuclear genes encoding mitochondrial proteins: isolation of a collection of D. melanogaster cDNAs homologous to sequences in the Human Gene Index database

7 January 2021

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Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing.

7 January 2021

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OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.08.013

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

7 January 2021

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The development of excitatory synapses in cultured spinal neurons

7 January 2021

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7 January 2021

Identifiers

DOI

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30 July 2017

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