Ann Indian Acad Neurol
 2018
DOI: 10.4103/aian.aian_106_18
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Hereditary spastic paraplegia type 35 with a novel mutation in fatty acid 2-hydroxylase gene and literature review of the clinical features

Faruk İncecik
1
,
Şeyda Beşen
2
,
Sevcan Tuğ Bozdoğan
3
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Cited by 6 publications
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References 18 publications
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The first reports of FA2H-associated neurodegeneration from two unrelated Iranian families

Hashemi
1
,
Abadi
2
,
Alavi
3
et al. 2023
Neurol Sci
3
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The first reports of FA2H-associated neurodegeneration from two unrelated Iranian families

Hashemi
1
,
Abadi
2
,
Alavi
3
et al. 2023
Neurol Sci
3
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0
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Identification of novel mutations by targeted NGS in Moroccan families clinically diagnosed with a neuromuscular disorder

Rochdi
1
,
Cerino
2
,
Silva
3
et al. 2022
Clinica Chimica Acta
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Exome sequencing of a Pakistani family with spastic paraplegia identified an 18 bp deletion in the cytochrome B5 domain of FA2H

Abbas
1
,
Brugger
2
,
Zubair
3
et al. 2020
Neurological Research
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