CareLit · DOI-Nachweis · Aktuelle Neurologie
Heritability of MRI lesion volume in CADASIL: evidence for genetic modifiers
DOI 10.1055/s-2006-953281
Bibliografische Angaben
Nachweis in CareLit
Autor:innenC. Opherk, N. Peters, M. Holtmannspötter, A. Gschwendtner, B. Müller-Myhsok, M. Dichgans
ZeitschriftAktuelle Neurologie
Ausgabe09/2006
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Objective: The severity of the phenotype varies markedly among individuals with CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy), a small vessel disease caused by mutations in NOTCH3. However, little is known about the factors underlying this variability. We sought to quantify the contribution of modifying genetic effects to individual differences in the volume of…
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Zitierempfehlung
C. Opherk, N. Peters, M. Holtmannspötter, A. Gschwendtner, B. Müller-Myhsok, M. Dichgans (2006) Heritability of MRI lesion volume in CADASIL: evidence for genetic modifiers. Aktuelle Neurologie (09). https://doi.org/10.1055/s-2006-953281
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