SPG20 - Wikipedia
Troyer Syndrome by Tanner Hall
Brain Sciences | Free Full-Text | Novel Type of Complicated Autosomal Dominant Hereditary Spastic Paraplegia Associated with Congenital Distal Arthrogryposis Type I
The perinatal phenotype of Troyer syndrome: Case report and literature review - Bryson - 2022 - American Journal of Medical Genetics Part A - Wiley Online Library
Morphological and radiological features of Omani individuals with... | Download Scientific Diagram
SPG20 Antikörper (ABIN570717)
Das Troyer-Syndrom -
Troyer syndrome: MedlinePlus Genetics
rare_diseases_in_pediatric_anesthesia
Das Troyer-Syndrom -
Homozygous frameshift mutation in TMCO1 causes a syndrome with craniofacial dysmorphism, skeletal anomalies, and mental retardation | PNAS
HSP : HSP & PLS : Spastic Paraplegia Foundation
Recurrent null mutation in SPG20 leads to Troyer syndrome - ScienceDirect
Troyer-Syndrom | pacs
Troyer syndrome: a combination of central brain abnormality and motor neuron disease?
TECPR2 mutations cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disability - ScienceDirect
Troyer syndrome: MedlinePlus Genetics
Three cases of Troyer syndrome in two families of Filipino descent - Butler - 2016 - American Journal of Medical Genetics Part A - Wiley Online Library
The Drosophila Odyssey: Spartin Insight into Troyer Syndrome - Knowing Neurons
Spastic paraplegia 20 (Troyer syndrome), IgG, Rabbit, Polyclonal | Labstore
PDF) Novel SPG20 mutation in an extended family with Troyer syndrome
What Is Troyer Syndrome? - StoryMD
Dwarfism in Troyer syndrome: a family with SPG20 compound heterozygous mutations and a literature review - Liang - 2020 - Annals of the New York Academy of Sciences - Wiley Online Library
The C-terminal region of SPG20 that is absent in the Troyer syndrome... | Download Scientific Diagram
Troyer syndrome // WoH Project // Exeter, Devon, United Kingdom
SPG20 Antibody (ABIN652983)
Troyer Syndrome by Tanner Hall
