Severe tangier disease with a novel ABCA1 gene mutation

Neurology

Volumn 71, Issue 18, 2008, Pages 1454-1455

  Schippling, S ^a   Orth, M ^a   Beisiegel, U ^a   Rosenkranz, T ^b   Vogel, P ^b   Munchau A ^a   Hagel, C ^a   Seedorf, U ^c  

^a UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^b DEPARTMENT OF CARDIOLOGY   (Germany)

^c UNIVERSITY OF MÜNSTER   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER A1; APOLIPOPROTEIN A1; HIGH DENSITY LIPOPROTEIN; HIGH DENSITY LIPOPROTEIN CHOLESTEROL; LOW DENSITY LIPOPROTEIN; ABC TRANSPORTER; CHOLESTEROL;

ADULT; AFGHANISTAN; ARTICLE; ATHEROSCLEROSIS; BRAIN ELECTROPHYSIOLOGY; CASE REPORT; CHOLESTEROL BLOOD LEVEL; CLINICAL EXAMINATION; DISEASE SEVERITY; DNA SEQUENCE; FAMILY; GENE MUTATION; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; LIPOPROTEIN BLOOD LEVEL; MALE; NERVE BIOPSY; PHENOTYPE; PRIORITY JOURNAL; SURAL NERVE; SYRINGOMYELIA; TANGIER DISEASE; GENETICS; METABOLISM; METHODOLOGY; MIDDLE AGED; MUTATION; NUCLEOTIDE SEQUENCE; PATHOLOGY;

ATP-BINDING CASSETTE TRANSPORTERS; CHOLESTEROL; DNA MUTATIONAL ANALYSIS; HUMANS; MALE; MIDDLE AGED; MUTATION; SURAL NERVE; TANGIER DISEASE;

EID: 58149237383     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/01.wnl.0000327870.29639.20     Document Type: Article

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