Infantile Dilated X-Linked Cardiomyopathy, G4.5 Mutations, Altered Lipids, and Ultrastructural Malformations of Mitochondria in Heart, Liver, and Skeletal Muscle

Strategies for multilocus linkage analysis in humans.

G.M. Lathrop, J.-M. Lalouel, Cécile Julier et al. · Proceedings of the National Academy of Sciences · 1984 · 2.6K citations · Full text

Life Sciences, Genetics, Genomics +16

Sequential tests for the detection of linkage.

Newton E. Morton · PubMed · 1955 · 1.6K citations

Life Sciences, Biostatistics, Genetics +8

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

Silvia Bione, Patrizia D’Adamo, Elena Maestrini et al. · Nature Genetics · 1996 · 752 citations

Life Sciences, Genetics, Molecular Genetics +6

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

P. G. Barth, H.R. Scholte, J.A. Berden et al. · Journal of the Neurological Sciences · 1983 · 701 citations

Medicine, Cardiology, Molecular Genetics +17

Novel Gene Mutations in Patients With Left Ventricular Noncompaction or Barth Syndrome

Fukiko Ichida, Shinichi Tsubata, Karla R. Bowles et al. · Circulation · 2001 · 558 citations

Medicine, Cardiology, Genetics +17