"
Wolman Disease in Bulgarian Patients: Selective Genetic Screening in Two Presumable Endemic Regions"
written by Angelina Mandadzhieva, Daniela Avdzhieva-Tzavella, Tihomir Todorov, Savina Tincheva, Vanya Sinigerska, Mariya Ivanova, Alexey Savov, Vanyo Mitev, Albena Todorova,
published by
American Journal of Molecular Biology,
Vol.7 No.4, 2017
has been cited by the following article(s):
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[1]
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Loss of lysosomal acid lipase results in mitochondrial dysfunction and fiber switch in skeletal muscles of mice
Molecular Metabolism,
2024
DOI:10.1016/j.molmet.2023.101869
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[2]
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First LIPA Mutational Analysis in Egyptian Patients Reveals One Novel Variant: Wolman Disease
Journal of Molecular Neuroscience,
2023
DOI:10.1007/s12031-023-02139-6
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[3]
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First LIPA Mutational Analysis in Egyptian Patients Reveals One Novel Variant: Wolman Disease
Journal of Molecular Neuroscience,
2023
DOI:10.1007/s12031-023-02139-6
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