Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: Clinical, biochemical, and molecular genetic features of the 1Oq-linked disease-Reference-Cited by-同舟云学术

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Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: Clinical, biochemical, and molecular genetic features of the 1Oq-linked disease

Published:1997-05-01 Issue:5 Volume:48 Page:1244-1253
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Suomalainen A.,Majander A.,Wallin M.,Setala K.,Kontula K.,Leinonen H.,Salmi T.,Paetau A.,Haltia M.,Valanne L.,Lonnqvist J.,Peltonen L.,Somer H.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

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