Differential diagnosis in spinal and bulbar muscular atrophy clinical and molecular aspects

Jöbsis, G.; Louwerse, Ilse; de Jong, Vianney; de Visser, Marianne; Wolterman, Ruud; Bolhuis, P.; Busch, Herman; Brüggenwirth, Hennie; Baas, Frank; Wiersinga, Wilmar; Koelman, Johannes

doi:10.1016/0022-510X(95)00064-9

Kennedy disease is caused by an enlarged trinucleotide repeat sequence within the androgen receptor gene. We report here seven male patients with a benign motor neuron syndrome highly analogous to Kennedy disease but with a normal trinucleotide repeat.

Additional Metadata
Keywords	Androgen receptor gene, Androgen sensitivity, Kennedy disease, Motor neuron disease, Trinucleotide repeat
Persistent URL	doi.org/10.1016/0022-510X(95)00064-9, hdl.handle.net/1765/66035
Journal	Journal of the Neurological Sciences
Organisation	Department of Neurology
Citation APA APA Style APA-ALL Style AAA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Jöbsis, G., Louwerse, I., de Jong, V., de Visser, M., Wolterman, R., Bolhuis, P., Busch, H., Brüggenwirth, H., Baas, F., Wiersinga, W.& Koelman, J. (1995). Differential diagnosis in spinal and bulbar muscular atrophy clinical and molecular aspects. Journal of the Neurological Sciences, 129(SUPPL.), 56–57.https://doi.org/10.1016/0022-510X(95)00064-9

Free Full Text ( Final Version , 176kb )

Differential diagnosis in spinal and bulbar muscular atrophy clinical and molecular aspects

Publication

Publication

About

Differential diagnosis in spinal and bulbar muscular atrophy clinical and molecular aspects

Publication

Publication

Workflow

Workflow

Add Content