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Bone changes in homocystinuria
Authors:J M MacCarthy  M C Carey
Affiliation:1. Equipe d''Accueil (EA 7460): Physiopathologie et Epidémiologie Cérébro-Cardiovasculaires (PEC2), Université de Bourgogne – Franche Comté, Faculté des Sciences de Santé, 7 Bd Jeanne d''Arc, 21000 Dijon, France;2. Service de Cardiologie, CHU, Dijon, France;1. Adult Inherited Metabolic Diseases, Salford Royal NHS Foundation Trust, UK;2. Department of Clinical Medicine, Marqués de Valdecilla University Hospital, López-Albo Post Residency Program, Santander, Spain;3. Clinical Genetics, Royal Liverpool Children Hospital, Alder Hey, Liverpool, UK;4. Ophthalmology Department, Warrington Hospital, Warrington, UK;5. Clinical Neuropsychology Department, Salford Royal Hospital NHS Foundation Trust, Salford, UK;6. Willink Metabolic Unit, St Mary''s Hospital, Manchester Foundation Trust, Manchester, UK;7. Warrington Primary Care Psychiatry, Warrington, UK;8. Neurology Department, Salford Royal Hospital NHS Foundation Trust, Salford, UK;9. Cardiology Department, Warrington Hospital, Warrington, UK;10. University of Pretoria, Steve Biko Academic Unit, Department of Paediatrics, Pretoria, South Africa;11. Division of Cardiovascular Sciences, University of Manchester, Manchester M13 9PL, UK
Abstract:
Keywords:
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