Annals of Indian Academy of Neurology
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1Case of Sjögren-Larsson syndrome with a large deletion in theALDH3A2gene confirmed by single nucleotide polymorphism array analysis
Nagwa E. A. Gaboon,Musharraf Jelani,Mona M. Almramhi,Hussein S. A. Mohamoud,Jumana Y. Al-Aama
The Journal of Dermatology.2015;42(7)706
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2A gatekeeper helix determines the substrate specificity of Sjögren–Larsson Syndrome enzyme fatty aldehyde dehydrogenase
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Nature Communications.2014;5(1)706
[DOI]
3Expanding the Genotype of Sjögren–Larsson Syndrome: A New Case Due to Two Novel Mutations
E. García-Peris,I. Latour-Álvarez,M. Pestana-Eliche,R. Sánchez
Actas Dermo-Sifiliográficas.2017;108(6)601
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4Expanding the Genotype of Sjögren–Larsson Syndrome: A New Case Due to Two Novel Mutations
E. García-Peris,I. Latour-Álvarez,M. Pestana-Eliche,R. Sánchez
Actas Dermo-Sifiliográficas (English Edition).2017;108(6)601
[DOI]
5Novel mutations and a severe neurological phenotype in Sjögren-Larsson syndrome patients from Iran
Ariana Kariminejad,Mohammadreza Barzgar,Bita Bozorgmehr,Elham Keshavarz,Mohamad Hasan Kariminejad,Dana S'Aulis,William B. Rizzo
European Journal of Medical Genetics.2018;61(3)139
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6Genotype and phenotype variability in Sjögren-Larsson syndrome
Maximilian Weustenfeld,Reiner Eidelpes,Matthias Schmuth,William B. Rizzo,Johannes Zschocke,Markus A. Keller
Human Mutation.2019;40(2)177
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7Understanding fetal factors that contribute to preterm birth: Sjögren-Larsson syndrome as a model
Pippa Staps,Marije Hogeveen,Joris Fuijkschot,Joris van Drongelen,Michèl A.A.P. Willemsen
Journal of Perinatal Medicine.2018;46(5)523
[DOI]
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