Generation of iPSC lines (KAIMRCi003A, KAIMRCi003B) from a Saudi patient with Dravet syndrome carrying homozygous mutation in the CPLX1 gene and heterozygous mutation in SCN9A
Alowaysi, Maryam, Al-Shehri, Mohammad, Badkok, Amani, Attas, Hanouf, Aboalola, Doaa, Baadhaim, Moayad, Alzahrani, Hajar, Daghestani, Mustafa, Zia, Asima, Al-Ghamdi, Khalid, Al-Ghamdi, Asayil, Zakri, Samer, Aouabdi, Sihem, Tegner, Jesper, Alsayegh, Khaled
Published in Human cell : official journal of Human Cell Research Society (01.03.2024)
Published in Human cell : official journal of Human Cell Research Society (01.03.2024)
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Journal Article
Derivation of two iPSC lines (KAIMRCi004-A, KAIMRCi004-B) from a Saudi patient with Biotin-Thiamine-responsive Basal Ganglia Disease (BTBGD) carrying homozygous pathogenic missense variant in the SCL19A3 gene
Alowaysi, Maryam, Baadhaim, Moayad, Al-Shehri, Mohammad, Alzahrani, Hajar, Badkok, Amani, Attas, Hanouf, Zakri, Samer, Alameer, Seham, Malibari, Dalal, Hosawi, Manal, Daghestani, Mustafa, Al-Ghamdi, Khalid, muharraq, Mohammed, Zia, Asima, Tegne, Jesper, Alfadhel, Majid, Aboalola, Doaa, Alsayegh, Khaled
Published in Human cell : official journal of Human Cell Research Society (01.09.2024)
Published in Human cell : official journal of Human Cell Research Society (01.09.2024)
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Journal Article
Generation of iPSC lines (KAIMRCi003A, KAIMRCi003B) from a Saudi patient with Dravet Syndrome carrying homozygous mutation in the CPLX1 gene and heterozygous mutation in SCN9A
Alowaysi, Maryam, Al-Shehri, Mohammad, Badkok, Amani, Attas, Hanouf, Aboalola, Doaa, Baadhaim, Moayad, Alzahrani, Hajar, Daghestani, Mustafa, Zia, Asima, Al-Ghamdi, Khalid, Al-Ghamdi, Asayil, Zakri, Samer, AOUABDI, SIHEM, Tegner, Jesper, Alsayegh, Khaled
Published in Research Square (Preprints) (04.10.2023)
Published in Research Square (Preprints) (04.10.2023)
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