Cysteine-sparing notch3 mutations: Cadasil or cadasil variants?

Neurology

Volumn 71, Issue 10, 2008, Pages 774-776

  Scheid, R ^a,c,d   Heinritz, W ^b   Leyhe, T ^e   Thal, D R ^f   Schober, R ^c,d   Strenge, S ^b   Von Cramon, D Y ^a,d   Froster, U G ^b  

^a Day Clinic of Cognitive Neurology   (Germany)

^b Department of Human Genetics ^*

^c UNIVERSITY OF LEIPZIG   (Germany)

^d MAX PLANCK INSTITUTE FOR HUMAN COGNITIVE AND BRAIN SCIENCES   (Germany)

^e UNIVERSITY OF TÜBINGEN   (Germany)

^f UNIVERSITY OF ULM   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

NOTCH3 RECEPTOR; CYSTEINE; NOTCH RECEPTOR; NOTCH3 PROTEIN, HUMAN;

ADULT; AGED; ARTICLE; BRAIN DAMAGE; CADASIL; CASE REPORT; COGNITIVE DEFECT; DISEASE ASSOCIATION; ELECTRON MICROSCOPY; FAMILY HISTORY; FEMALE; HEADACHE; HEARING LOSS; HUMAN; HUMAN TISSUE; HYPERTENSION; IMMUNOHISTOCHEMISTRY; LIMB WEAKNESS; MALE; MEMORY DISORDER; MISSENSE MUTATION; NAUSEA; NUCLEAR MAGNETIC RESONANCE IMAGING; PARESTHESIA; PERCEPTION DEAFNESS; PRIORITY JOURNAL; SKIN BIOPSY; VERTIGO; WHITE MATTER; GENETICS; MIDDLE AGED; MUTATION; NUCLEOTIDE SEQUENCE; PATHOLOGY;

AGED; CADASIL; CYSTEINE; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; MIDDLE AGED; MUTATION; RECEPTORS, NOTCH;

EID: 54049156527     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/01.wnl.0000324928.44694.f7     Document Type: Article

References (7)

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