X-linked sideroblastic anaemia with ataxia: Another mitochondrial disease?

Journal of Neurology Neurosurgery and Psychiatry

Volumn 70, Issue 1, 2001, Pages 65-69

  Hellier, K D ^a   Hatchwell, E ^b   Duncombe, A S ^c   Kew, J ^c   Hammans, S R ^a  

^a SOUTHAMPTON GENERAL HOSPITAL   (United Kingdom)

^b Wessex Human Genetics Institute   (United Kingdom)

^c PRINCESS ROYAL HOSPITAL   (United Kingdom)

Author keywords

Ataxia; Sideroblastic anaemia

Indexed keywords

ABC TRANSPORTER; ERYTHROCYTE PROTOPORPHYRIN; GENE PRODUCT; IRON;

ADULT; AGED; ANEMIA; ARTICLE; ATAXIA; BLOOD CELL COUNT; BONE MARROW EXAMINATION; CASE REPORT; CLINICAL FEATURE; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DYSARTHRIA; FAMILIAL DISEASE; FEMALE; FRIEDREICH ATAXIA; GENDER; GENETIC ANALYSIS; HUMAN; IRON BLOOD LEVEL; IRON TRANSPORT; MALE; MOTOR DEVELOPMENT; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PATHOPHYSIOLOGY; PEARSON SYNDROME; PRIORITY JOURNAL; SIDEROBLASTIC ANEMIA; SPASTICITY; X CHROMOSOME LINKED DISORDER;

EID: 0035137838     PISSN: 00223050     EISSN: None     Source Type: Journal    
DOI: 10.1136/jnnp.70.1.65     Document Type: Article

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