Cargando…
Genetic Spectrum of Inherited Neuropathies in India
BACKGROUND AND OBJECTIVES: Charcot-Marie-Tooth (CMT) disease is the commonest inherited neuromuscular disorder and has heterogeneous manifestations. Data regarding genetic basis of CMT from India is limited. This study aims to report the variations by using high throughput sequencing in Indian CMT c...
Autores principales: | Sharma, Shivani, Govindaraj, Periyasamy, Chickabasaviah, Yasha T., Siram, Ramesh, Shroti, Akhilesh, Seshagiri, Doniparthi V., Debnath, Monojit, Bindu, Parayil S., Taly, Arun B., Nagappa, Madhu |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9350795/ https://www.ncbi.nlm.nih.gov/pubmed/35936615 http://dx.doi.org/10.4103/aian.aian_269_22 |
Ejemplares similares
-
An uncommon cause of bifacial weakness and non-length-dependent demyelinating neuropathy
por: Nagappa, Madhu, et al.
Publicado: (2015) -
Tangier's disease: An uncommon cause of facial weakness and non-length dependent demyelinating neuropathy
por: Nagappa, Madhu, et al.
Publicado: (2016) -
Impact of Antecedent Infections on the Antibodies against Gangliosides and Ganglioside Complexes in Guillain-Barré Syndrome: A Correlative Study
por: Dutta, Debprasad, et al.
Publicado: (2022) -
Clinical, hematological, and imaging observations in a 25-year-old woman with abetalipoproteinemia
por: Nagappa, Madhu, et al.
Publicado: (2014) -
Vogt-Koyanagi-Harada Syndrome - A Neurologist's Perspective
por: Shivaram, Sumanth, et al.
Publicado: (2021)