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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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U Dillmann

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American Journal of Human Genetics|May 11, 2006

Mutations in the gene encoding peroxisomal sterol carrier protein X (SCPx) cause leukencephalopathy with dystonia and motor neuropathyS Ferdinandusse, P Kostopoulos, S Denis, et al.

BMJ Case Reports|June 21, 2011

A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathyAn I Jonckheere, Marije Hogeveen, Leo Nijtmans, et al.

Journal of Medical Genetics|October 24, 2007

A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathyA I Jonckheere, M Hogeveen, L G J Nijtmans, et al.

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Search research articles

Showing results (31-40 of 33) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 33 results.

American Journal of Human Genetics|May 11, 2006

Mutations in the gene encoding peroxisomal sterol carrier protein X (SCPx) cause leukencephalopathy with dystonia and motor neuropathyS Ferdinandusse, P Kostopoulos, S Denis, et al.

BMJ Case Reports|June 21, 2011

A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathyAn I Jonckheere, Marije Hogeveen, Leo Nijtmans, et al.

Journal of Medical Genetics|October 24, 2007

A novel mitochondrial ATP8 gene mutation in a patient with apical hypertrophic cardiomyopathy and neuropathyA I Jonckheere, M Hogeveen, L G J Nijtmans, et al.

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