Article
[TK2 mutations and late onset myopathy: first description in a Mexican patient].
Revista de neurologia - 16 Sept 2018
Castro-Macias J I, Quijas-Aldana I, Diaz-Campos M O, Santos-Vazquez G, Normendez-Martinez M, San-Juan D, Anschel D J
Abstract excerpt
TITLE: Mutacion del gen TK2 y miopatia de inicio tardio: descripcion del primer caso mexicano.
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
