Severe encephalomyopathy in a patient with homoplasmic A5814G point mutation in mitochondrial tRNACys gene

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Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis
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Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis

Published on: June 9, 2018

Carmela Scuderi1, Eugenia Borgione, Sebastiano Musumeci

  • 1Dipartimento di Neurologia, IRCCS Oasi Maria SS, Troina, Italy. cscuderi@oasi.en.it

Neuromuscular Disorders : NMD
|January 24, 2007
PubMed

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