Work

Dominantly inherited proximal myotonic myopathy and leuco-encephalopathy in a family with an incidental CLCN 1 mutation

Year: 1997

Type: other

Source: UWA Profiles and Research Repository (UWA)

Authors: Mastaglia, F., Harker, N., Phillips, B., Day, T., Hankey, G.; id_orcid 0000-0002-6044-7328, Fabian, V., Laing, Nigel; id_orcid 0000-0001-5111-3732

Institution: The University of Western Australia

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: W2618256376

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Related to: 10