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absence of mtdna mutations in leukocytes of cadasil patients缺乏mtdna突变cadasil患者的白细胞
BMC Research Notes BioMed Central
Short Report Open Access
Absence of mtDNA mutations in leukocytes of CADASIL patients
1,4 2 3
Khaled K Abu-Amero* , Ali Hellani and Saeed Bohlega
Address: 1Mitochondrial Research Laboratory, Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia,
2PGD laboratory, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia, 3Neuroscience department, King Faisal Specialist
Hospital and Research Center, Riyadh, Saudi Arabia and 4King Faisal Specialist Hospital, PO Box 3354, Riyadh, KSA, Saudi Arabia
Email: Khaled K Abu-Amero* - abuamero@; Ali Hellani - alihellani@; Saeed Bohlega - bohlega@.sa
* Corresponding author
Published: 30 May 2008 Received: 1 May 2008
Accepted: 30 May 2008
BMC Research Notes 2008, 1:16 doi:10.1186/1756-0500-1-16
This article is available from: /1756-0500/1/16
© 2008 Abu-Amero et al; licensee BioMed Central Ltd.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (/licenses/by/2.0),
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract
Background: Ultrastructural and biochemical abnormalities of mitochondria have been reported
in skeletal muscle biopsies of CADASIL patients with mutations in the NOTCH3 nuclear gene.
Additionally, it was proposed that NOTCH3 gene
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