Author:
Wortmann Saskia B.,Kluijtmans Leo A.,Engelke Udo F. H.,Wevers Ron A.,Morava Eva
Subject
Genetics(clinical),Genetics
Reference79 articles.
1. Adwani SS, Whitehead BF, Rees PG et al (1997) Heart transplantation for Barth syndrome. Pediatr Cardiol 18(2):143–145
2. Anikster Y, Kleta R, Shaag A et al (2001) Type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi Jews. Am J Hum Genet 69(6):1218–1224
3. Barth PG, Van't Veer-Korthof ET, Van Delden L et al (1981) An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leukocytes. In: Busch HFM, Jennekens FGI, Schotte HR (eds) Mitochondria and Muscular Diseases. Beetsterzwaag: 161–164
4. Barth PG, Scholte JA, Berden JA, Van der Klei-Van Moorsel JM et al (1983) An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes. J Neurol Sci 62:327–355
5. Barth PG, Valianpour F, Bowen VM et al (2004) X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): an update. Am J Med Genet A 126A(4):349–354
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