Intrathecal gene therapy in mouse models expressing CMT1X mutations-Reference-Cited by-同舟云学术

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Intrathecal gene therapy in mouse models expressing CMT1X mutations

Published:2018-02-14 Issue:8 Volume:27 Page:1460-1473
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Kagiava A¹,Karaiskos C¹,Richter J²,Tryfonos C²,Lapathitis G¹,Sargiannidou I¹,Christodoulou C²,Kleopa K A¹³

Affiliation:

1. Neuroscience Laboratory, The Cyprus Institute of Neurology and Genetics, Cyprus School of Molecular Medicine, 1683 Nicosia, Cyprus

2. Department of Molecular Virology, The Cyprus Institute of Neurology and Genetics, Cyprus School of Molecular Medicine, 1683 Nicosia, Cyprus

3. Neurology Clinics, The Cyprus Institute of Neurology and Genetics, Cyprus School of Molecular Medicine, 1683 Nicosia, Cyprus

Funder

Muscular Dystrophy Association

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/27/8/1460/24527136/ddy056.pdf

Reference44 articles.

1. Connexin mutations in X-linked Charcot-Marie-Tooth disease;Bergoffen;Science,1993

2. Clinical, electrophysiological and molecular genetic characteristics of 93 patients with X-linked Charcot-Marie-Tooth disease;Dubourg;Brain,2001

3. Mutations of the noncoding region of the connexin32 gene in X-linked dominant Charcot-Marie-Tooth neuropathy;Ionasescu;Neurology,1996

4. Functional gap junctions in the schwann cell myelin sheath;Balice-Gordon;J. Cell Biol,1998

5. Molecular genetics of X-linked Charcot-Marie-Tooth disease;Kleopa;Neuromolecular Med,2006

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