Spinal Muscular Atrophy Carrier Frequency and Estimated Prevalence of the Disease in Moroccan Newborns-Reference-Cited by-同舟云学术

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Spinal Muscular Atrophy Carrier Frequency and Estimated Prevalence of the Disease in Moroccan Newborns

Published:2012-03 Issue:3 Volume:16 Page:215-218
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Lyahyai Jaber¹²,Sbiti Aziza²,Barkat Amina³,Ratbi Ilham¹²,Sefiani Abdelaziz¹²

Affiliation:

1. Centre de Génomique Humaine, Faculté de Médecine et Pharmacie, Université Mohamed V Souissi, Rabat, Morocco.

2. Département de Génétique Médicale, Institut National d'Hygiène, Rabat, Morocco.

3. Centre National de Référence en Néonatologie et en Nutrition, Rabat, Morocco.

Publisher

Mary Ann Liebert Inc

Subject

Genetics(clinical),General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2011.0149

Reference26 articles.

1. Prevalence of type I spinal muscular atrophy in North Dakota

2. Consanguinity, fertility of couples and mortality of children in the high Atlas population (commons of Anougal and Azgour, Marrakesh, Morroco)

3. New Approaches in Molecular Diagnosis and Population Carrier Screening for Spinal Muscular Atrophy

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3. Real-world evidence: Risdiplam in a patient with spinal muscular atrophy type I with a novel splicing mutation and one SMN2 copy;Human Molecular Genetics;2024-03-23

4. Spinal muscular atrophy genetic epidemiology and the case for premarital genomic screening in Arab populations;2024-01-16

5. Carrier screening for spinal muscular atrophy in 22913 Chinese reproductive age women;Molecular Genetics & Genomic Medicine;2024-01

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