A therapeutic role for hematopoietic stem cells in osteogenesis imperfecta; Laminopathies; Hutchinson gilford progeria syndrome; Genetic determinants of heart rate variation and cardiovascular diseases; Structural insights into disease mutations of the ryanodine receptor; Epilepsy and genetics; Rett syndrome: A model of genetic neurodevelopmental disorders; Genetics and obesity; Bone marrow microenvironment defects in fanconi anemia; Cystic fibrosis: Does CFTR malfunction alter pH.
