Articles with "dstdt" as a keyword



Dystonin‐A3 upregulation is responsible for maintenance of tubulin acetylation in a less severe dystonia musculorum mouse model for hereditary sensory and autonomic neuropathy type VI

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Published in 2018 at "Human Molecular Genetics"

DOI: 10.1093/hmg/ddy250

Abstract: Abstract Hereditary sensory and autonomic neuropathy type VI (HSAN‐VI) is a recessive human disease that arises from mutations in the dystonin gene (DST; also known as Bullous pemphigoid antigen 1 gene). A milder form of… read more here.

Keywords: tubulin acetylation; dst; dstdt tg4; dstdt ... See more keywords