Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26-Reference-Cited by-同舟云学术

Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26

Published:2015-11 Issue:5 Volume:97 Page:761-768
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Kishita Yoshihito,Pajak Aleksandra,Bolar Nikhita Ajit,Marobbio Carlo M.T.,Maffezzini Camilla,Miniero Daniela V.,Monné Magnus,Kohda Masakazu,Stranneheim Henrik,Murayama Kei,Naess Karin,Lesko Nicole,Bruhn Helene,Mourier Arnaud,Wibom Rolf,Nennesmo Inger,Jespers Ann,Govaert Paul,Ohtake Akira,Van Laer Lut,Loeys Bart L.,Freyer Christoph,Palmieri Ferdinando,Wredenberg Anna,Okazaki Yasushi,Wedell Anna

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference32 articles.

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3. Protein methylation at the surface and buried deep: thinking outside the histone box;Clarke;Trends Biochem. Sci.,2013

4. Identification of the human mitochondrial S-adenosylmethionine transporter: bacterial expression, reconstitution, functional characterization and tissue distribution;Agrimi;Biochem. J.,2004

5. Stranneheim, H. (2014). Mutation Identification Pipeline (MIP), https://github.com/henrikstranneheim/MIP.

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