(Q27936025)

1 December 2016

title

Barth syndrome may be due to an acyltransferase deficiency (English)

1 reference

PubMed

Putative acyltransferase YDR018C

1 December 2016

main subject

1 reference

GOA release 2020-03-11

Mum3p YOR298W

1 reference

GOA release 2020-03-11

1 reference

A. F. Neuwald

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9259571

full work available at URL

11 November 2024

language of work or name

English

0 references

publication date

1 August 1997

0 references

http://www.cell.com/article/S0960982206002375/pdf

file format

Portable Document Format

online access status

open access

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9259571

https://api.elsevier.com/content/article/PII:S0960982206002375?httpAccept=text/xml

11 November 2024

1 reference

https://api.crossref.org/works/10.1016/S0960-9822(06)00237-5

https://api.elsevier.com/content/article/PII:S0960982206002375?httpAccept=text/plain

11 November 2024

1 reference

https://api.crossref.org/works/10.1016/S0960-9822(06)00237-5

11 November 2024

1 reference

X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): respiratory-chain abnormalities in cultured fibroblasts

1 December 2016

volume

7

0 references

issue

8

0 references

page(s)

R465-6

0 references

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2806%2900237-5

7 January 2021

An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2806%2900237-5

7 January 2021

Endocardial fibroelastosis: possible X linked inheritance

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2806%2900237-5

7 January 2021

Possible X linked congenital mitochondrial cardiomyopathy in three families

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2806%2900237-5

7 January 2021

X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2806%2900237-5

7 January 2021

A novel X-linked gene, G4.5. is responsible for Barth syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2806%2900237-5

7 January 2021

Basic local alignment search tool

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2806%2900237-5

7 January 2021

Extracting protein alignment models from the sequence database

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2806%2900237-5

7 January 2021

Structure of chloramphenicol acetyltransferase at 1.75-A resolution

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2806%2900237-5

7 January 2021

Positionally cloned human disease genes: patterns of evolutionary conservation and functional motifs

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2806%2900237-5

7 January 2021

Gibbs motif sampling: detection of bacterial outer membrane protein repeats

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2806%2900237-5

7 January 2021

Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28

series ordinal

6

1 reference

https://api.crossref.org/works/10.1016/S0960-9822(06)00237-5

11 November 2024

Identifiers

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017