Zobrazeno 1 - 2
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pro vyhledávání: '"Petros Toulios"'
Autor:
Vasileios Papaliagkas, Nikolaos Foroglou, Petros Toulios, Maria Moschou, Maria Gavriilaki, Konstantinos Notas, Evangelia Chatzikyriakou, Georgia Zafeiridou, Marianthi Arnaoutoglou, Vasilios K. Kimiskidis
Publikováno v:
Case Reports in Neurology, Vol 13, Iss 3, Pp 710-715 (2021)
Spinal muscular atrophy (SMA) is a hereditary neuromuscular disorder, typically caused by survival motor neuron 1 (SMN1) gene deletion in chromosome 5q resulting in loss of SMN protein. SMA type 1 progresses rapidly leading to increased mortality usu
Externí odkaz:
https://doaj.org/article/bd7d33fc23a84cec8040e955230bfb92
Autor:
Maria Gavriilaki, Konstantinos Notas, Vasileios Papaliagkas, Evangelia Chatzikyriakou, Marianthi Arnaoutoglou, Vasilios K. Kimiskidis, Georgia Zafeiridou, Maria Moschou, Nikolaos Foroglou, Petros Toulios
Publikováno v:
Case Reports in Neurology, Vol 13, Iss 3, Pp 710-715 (2021)
Case Reports in Neurology
Case Reports in Neurology
Spinal muscular atrophy (SMA) is a hereditary neuromuscular disorder, typically caused by survival motor neuron 1 (SMN1) gene deletion in chromosome 5q resulting in loss of SMN protein. SMA type 1 progresses rapidly leading to increased mortality usu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93ebb52e2439fee97af4a0a0b00b22e3
https://doi.org/10.1159/000519831
https://doi.org/10.1159/000519831