Genetic Counselling for Maternally Inherited Mitochondrial Disorders-Reference-Cited by-同舟云学术

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Genetic Counselling for Maternally Inherited Mitochondrial Disorders

Published:2017-05-23 Issue:4 Volume:21 Page:419-429
ISSN:1177-1062
Container-title:Molecular Diagnosis & Therapy
language:en
Short-container-title:Mol Diagn Ther

Author:

Poulton Joanna,Finsterer Josef,Yu-Wai-Man Patrick

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology,Genetics,Molecular Medicine,General Medicine

Link

http://link.springer.com/article/10.1007/s40291-017-0279-7/fulltext.html

Reference92 articles.

1. Parikh S, Goldstein A, Keening MK, Scaglia F, Enns GM, Saneto R, et al. Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society. Genet Med. 2015;17:689–701.

2. Gorman G, Schaefer A, Ng Y, Gomez N, Blakely EL, Alston CL, et al. Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease. Ann Neurol. 2015;77:753–9.

3. Nesbitt V, Alston CL, Blakely EL, Fratter C, Feeney CL, Poulton J, et al. A national perspective on prenatal testing for mitochondrial disease. Eur J Hum Genet. 2014;22:1255–9.

4. Manwaring N, Jones MM, Wang JJ, Rochtchina E, Howard C, Mitchell P, Sue CM. Population prevalence of the MELAS A3243G mutation. Mitochondrion 2007;7:230–3.

5. Vento JM, Pappa B. Genetic counseling in mitochondrial disease. Neurotherapeutics. 2013;10:243–50.

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