Mitochondrial protein alterations in a familial peripheral neuropathy caused by the V144D amino acid mutation in the sphingolipid protein, SPTLC1
Crossref DOI link: https://doi.org/10.1007/s12154-014-0125-x
Published Online: 2014-11-14
Published Print: 2015-01
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Stimpson, Scott E.
Coorssen, Jens R.
Myers, Simon J.
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