X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060)-Reference-Cited by-同舟云学术

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X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060)

Published:1999-06 Issue:4 Volume:22 Page:555-567
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Barth P. G.¹²,Wanders R. J. A.¹³,Vreken P.¹³,Janssen E. A. M.²,Lam J.¹,Baas F.²

Affiliation:

1. ; Emma Children's Hospital, Department of Pediatrics; Amsterdam The Netherlands; and

2. ; Department of Neurology; University Hospital Amsterdam; Amsterdam The Netherlands

3. ; Department of Clinical Chemistry; Academic Medical Centre; Amsterdam The Netherlands

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005568609936/fullpdf

Reference44 articles.

1. Barth syndrome: clinical features and confirmation of gene localisation to distal Xq28;Adès;Am J Med Genet,1993

2. Heart transplantation for dilated cardiomyopathy;Adwani;Arch Dis Child,1995

3. 3-Methylglutaconic aciduria: ten new cases with a possible new phenotype;Al Aqeel;Brain Dev,1994

4. 3-Methylglutaconic aciduria in a patient with a disturbed mitochondrial energy metabolism [Letter];Bakkeren;Eur J Pediatr,1992

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2. Neutropenia in Childhood—A Narrative Review and Practical Diagnostic Approach;Hematology Reports;2024-06-16

3. Tafazzin deficiency causes substantial remodeling in the lipidome of a mouse model of Barth Syndrome cardiomyopathy;Frontiers in Molecular Medicine;2024-04-29

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