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Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients
by
Amara, Abdelbasset
,
Adala, Labiba
,
Ben Charfeddine, Ilhem
,
Mamaï, Ons
,
Mili, Amira
,
Lazreg, Taheni Ben
,
H’mida, Dorra
,
Amri, Fathi
,
Salem, Najla
,
Boughammura, Lamia
,
Saad, Ali
,
Gribaa, Moez
Published in
European journal of paediatric neurology
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Correlation of SMN 2, NAIP , p44 , H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients
by
Amara, Abdelbasset
,
Adala, Labiba
,
Ben Charfeddine, Ilhem
,
Mamaï, Ons
,
Mili, Amira
,
Lazreg, Taheni Ben
,
H’mida, Dorra
,
Amri, Fathi
,
Salem, Najla
,
Boughammura, Lamia
,
Saad, Ali
,
Gribaa, Moez
Published in
European journal of paediatric neurology
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Article
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European Journal Of Paediatric Neurology
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Pediatrics
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Adolescent
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Child
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Child, Preschool
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Chromosomes, Human, Pair 5 - Genetics
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Clinical Neurology
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Copy Number
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Exons - Genetics
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Female
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Gene Deletion
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Gene Dosage
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Genotype
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H4F5
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Humans
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Infant
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Life Sciences & Biomedicine
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Male
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Membrane Proteins - Genetics
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Mlpa
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Multiplex Polymerase Chain Reaction
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Sciencedirect®
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Sciencedirect Freedom Collection 2022-2024
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Science Citation Index Expanded (Web Of Science)
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Ingentaconnect Journals
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