Pelizaeus-Merzbacher-Like disease presentation of MCT8 mutated male subjects-Reference-Cited by-同舟云学术

Pelizaeus-Merzbacher-Like disease presentation of MCT8 mutated male subjects

Published:2009-02-04 Issue:1 Volume:65 Page:114-118
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Vaurs-Barrière Catherine,Deville Marlène,Sarret Catherine,Giraud Geneviève,Des Portes Vincent,Prats-Viñas José-Maria,De Michele Giuseppe,Dan Bernard,Brady Angela F.,Boespflug-Tanguy Odile,Touraine Renaud

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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3. GJA12 mutations are a rare cause of Pelizaeus-Merzbacher-like disease;Henneke;Neurology,2008

4. A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter gene;Dumitrescu;Am J Hum Genet,2004

5. Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation;Friesema;Lancet,2004

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