Museer A. Lone
University Hospital of Zurich
28 papers found
Refreshing results…
CERT1 mutations perturb human development by disrupting sphingolipid homeostasis
Download from doi.orgChildhood amyotrophic lateral sclerosis caused by excess sphingolipid synthesis
Download from www.nature.comA Novel Variant (Asn177Asp) in SPTLC2 Causing Hereditary Sensory Autonomic Neuropathy Type 1C
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