Barth syndrome mutations. Medical search. Frequent questions

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Anatomy1

Mitochondrial Membranes

Diseases13

Barth Syndrome Syndrome Genetic Diseases, X-Linked Cardiomyopathy, Dilated Muscular Diseases Andersen Syndrome Long QT Syndrome Craniosynostoses Cardiomyopathies LEOPARD Syndrome Noonan Syndrome Growth Disorders Neutropenia

Chemicals and Drugs6

Cardiolipins Glutarates 1-Acylglycerophosphocholine O-Acyltransferase NAV1.5 Voltage-Gated Sodium Channel Transcription Factors Lysophospholipids

Analytical, Diagnostic and Therapeutic Techniques and Equipment1

Phenomena and Processes3

Mutation Mutation, Missense Point Mutation

Anatomy Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes

Barth Syndrome Syndrome Cardiolipins Genetic Diseases, X-Linked Glutarates Mutation Mutation, Missense Cardiomyopathy, Dilated Muscular Diseases Point Mutation 1-Acylglycerophosphocholine O-Acyltransferase Andersen Syndrome Long QT Syndrome Craniosynostoses Cardiomyopathies LEOPARD Syndrome NAV1.5 Voltage-Gated Sodium Channel Mitochondrial Membranes Pedigree Noonan Syndrome Growth Disorders Neutropenia Transcription Factors Lysophospholipids

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