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Brain, ISSN 0006-8950, 04/2016, Volume 139, Issue 4, pp. e26 - e26
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2015, Volume 10, Issue 4, p. e0124232
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 03/2018, Volume 102, Issue 3, pp. 505 - 514
Journal Article
Journal of Clinical Neuroscience, ISSN 0967-5868, 01/2019, Volume 59, pp. 337 - 339
Biallelic pathogenic variants in gene have been repeatedly described as a cause of hereditary spastic paraplegia (HSP) type35 (SPG35). Targeted massive... 
Hereditary spastic paraplegia | FA2H gene | SPG35 | NEUROSCIENCES | CLINICAL NEUROLOGY | Spastic Paraplegia, Hereditary - genetics | Homozygote | Pedigree | Humans | Adult | Male | Spastic Paraplegia, Hereditary - pathology | Mutation | Mixed Function Oxygenases - genetics | Genes, Recessive
Journal Article
International Journal of Pediatric Otorhinolaryngology, ISSN 0165-5876, 2012, Volume 76, Issue 11, pp. 1681 - 1684
Journal Article
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