Work

Proteome alterations associated with the V144D SPTLC1 mutation that causes hereditary sensory neuropathy-I

Year: 2015

Type: article

Source: Electronic journal of biology

Authors: Scott E. Stimpson, Jens R. Coorssen, Simon J. Myers

Language: English

Topic: Hereditary Neurological Disorders

Subfield: Cellular and Molecular Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2344914976

FWCI: 0.125

Cites: 31

Cited by: 1

Related to: 10