Zobrazeno 1 - 3
of 3
pro vyhledávání: '"John L. Rodda"'
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Spinal muscular atrophy (SMA) is a neuromuscular disorder, characterized by muscle atrophy and impaired mobility. A homozygous deletion of survival motor neuron 1 (SMN1), exon 7 is the main cause of SMA in ~94% of patients worldwide, but only account
Externí odkaz:
https://doaj.org/article/80b70e73099a4d83a0ea8087ae1246c6
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Frontiers in Genetics
Frontiers in Genetics
Spinal muscular atrophy (SMA) is a neuromuscular disorder, characterized by muscle atrophy and impaired mobility. A homozygous deletion of survival motor neuron 1 (SMN1), exon 7 is the main cause of SMA in ~94% of patients worldwide, but only account
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6296d73b65501b3975daaced0a55e106
https://www.frontiersin.org/article/10.3389/fgene.2020.00054/full
https://www.frontiersin.org/article/10.3389/fgene.2020.00054/full
Publikováno v:
South African Medical Journal. 105:897
Acute ataxia in childhood is often caused by toxin ingestion. With the increasing number of paediatric patients on antiretroviral medication, we observe more side-effects of these drugs. Acute ataxia is defined as unsteadiness of walking or fine moto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd604617f86f6b9edd8b80fdc64f6805
https://doi.org/10.7196/samj.2015.v105i11.9451
https://doi.org/10.7196/samj.2015.v105i11.9451