Neurologic features and genotype-phenotype correlation in Wolfram syndrome

Annals of Neurology

Volumn 69, Issue 3, 2011, Pages 501-508

  Chaussenot, Annabelle ^a   Bannwarth, Sylvie ^a,b   Rouzier, Cecile ^a,b   Vialettes, Bernard ^c   Mkadem, Samira Ait El ^a,b   Chabrol, Brigitte ^c   Cano, Aline ^c   Labauge, Pierre ^d   Paquis Flucklinger, Véronique ^a,b  

^a CENTRE HOSPITALIER UNIVERSITAIRE DE NICE   (France)

^b UNIVERSITY OF NICE SOPHIA ANTIPOLIS   (France)

^c TIMONE HOSPITAL   (France)

^d NÎMES UNIVERSITY HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BRAIN MALFORMATION; CHILD; CISD2 GENE; CLINICAL FEATURE; COGNITIVE DEFECT; EPILEPSY; FEMALE; GENE; GENE MUTATION; GENOTYPE PHENOTYPE CORRELATION; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; INDEL MUTATION; LEUKOENCEPHALOPATHY; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; NEUROLOGIC DISEASE; NONSENSE MUTATION; NUCLEAR MAGNETIC RESONANCE IMAGING; ONSET AGE; PRIORITY JOURNAL; WFS1 GENE; WOLFRAM SYNDROME;

ADOLESCENT; ADULT; AGE FACTORS; ALLELES; CHILD; COGNITION DISORDERS; EPILEPSY; FEMALE; GENETIC ASSOCIATION STUDIES; HUMANS; MALE; MEMBRANE PROTEINS; MUTATION; NERVOUS SYSTEM DISEASES; WOLFRAM SYNDROME;

EID: 79953273922     PISSN: 03645134     EISSN: 15318249     Source Type: Journal    
DOI: 10.1002/ana.22160     Document Type: Article

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