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First LIPA Mutational Analysis in Egyptian Patients Reveals One Novel Variant: Wolman Disease

Nesma M. Elaraby,Eman Reda Galal,Mohamed Abdel-Hamid,Hasnaa M. Elbendary,Mohamed Elbadry,Mona K. Mekkawy,Neveen A. Ashaat,Samir M. Mounir,Engy A. Ashaat

JOURNAL OF MOLECULAR NEUROSCIENCE（2023）

Cited 0|Views15
Key words
Wolman disease,Lysosomal acid lipase deficiency,LIPA gene,Novel variant
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