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Oryzias latipes (JAPANESE MEDAKA) AS GENETIC MODEL TO STUDY CAUSATIVE GENES OF EPILEPSY DISEASE: AN IN-SILICO APPROACH

by MOHAMED YUNUS, NORFATIMAH, MAT YUSUF, UMI NABILA, AHMAD, LYENA WATTY ZURAINE, KAMBOL, ROZIAH, ARIS, FARIZAN, ZAKARIA, NURUL AILI
Published in Malaysian applied biology (31.10.2022)

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Frameshift mutation of LAMP2:c.667delT in a 17-year-old male with hypertrophic cardiomyopathy and dyslexia: a novel pathogenic variant for Danon disease

by Sani, Huzairi, Teh, Lay Kek, Noorizhab, Mohd Nur Fakhruzzaman, Zainal Abidin, Norzuliana, Mat Yusuf, Umi Nabila, Zulkufli, Nada Syazana, Kasim, Sazzli, Salleh, Mohd Zaki
Published in Singapore medical journal (09.05.2024)

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Frameshift mutation of LAMP2:c.667delT in a 17-year-old male with hypertrophic cardiomyopathy and dyslexia: a novel pathogenic variant for Danon disease

by Sani, Huzairi, Teh, Lay Kek, Noorizhab, Mohd Nur Fakhruzzaman, Zainal Abidin, Norzuliana, Mat Yusuf, Umi Nabila, Zulkufli, Nada Syazana, Kasim, Sazzli, Salleh, Mohd Zaki
Published in Singapore medical journal (09.05.2024)

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Journal Article

Oryzias latipes (JAPANESE MEDAKA) AS GENETIC MODEL TO STUDY CAUSATIVE GENES OF EPILEPSY DISEASE: AN IN-SILICO APPROACH

Frameshift mutation of LAMP2:c.667delT in a 17-year-old male with hypertrophic cardiomyopathy and dyslexia: a novel pathogenic variant for Danon disease

Frameshift mutation of LAMP2:c.667delT in a 17-year-old male with hypertrophic cardiomyopathy and dyslexia: a novel pathogenic variant for Danon disease

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