LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency-Reference-Cited by-同舟云学术

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LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency

Published:2011-01-25 Issue:3 Volume:48 Page:183-189
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Debray F.-G.,Morin C.,Janvier A.,Villeneuve J.,Maranda B.,Laframboise R.,Lacroix J.,Decarie J.-C.,Robitaille Y.,Lambert M.,Robinson B. H.,Mitchell G. A.

Publisher

BMJ

Subject

Genetics (clinical),Genetics

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