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Search Results - Al-Muhaizea, Muhammad
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Novel V97G ASAH1 mutation found in Farber disease patients: Unique appearance of the disease with an intermediate severity, and marked early involvement of central and peripheral n...
by
Chedrawi, Aziza K
,
Al-Hassnan, Zuhair N
,
Al-Muhaizea, Muhammad
,
Colak, Dilek
,
Al-Younes, Banan
,
Albakheet, AlBandary
,
Tulba, Sahar
,
Kaya, Namik
Published in
Brain & development (Tokyo. 1979)
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Brain & Development
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Acid Ceramidase - Genetics
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Asah1
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Brain - Pathology
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Child, Preschool
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Clinical Neurology
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Farber Disease
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Farber Lipogranulomatosis - Genetics
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Farber Lipogranulomatosis - Pathology
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Female
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Humans
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Infant
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Magnetic Resonance Imaging
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Sciencedirect Freedom Collection 2022-2024
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