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Browsing by Author Quek, Debra QY

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	Issue Date	Title	Author(s)
	26-Jun-2015	A partially inactivating mutation in the sodium-dependent lysophosphatidylcholine transporter MFSD2A causes a non-lethal microcephaly syndrome	Alakbarzade, Vafa; Hameed, Abdul; Quek, Debra QY; Chioza, Barry A; Baple, Emma L; Cazenave-Gassiot, Amaury; Nguyen, Long N; Wenk, Markus R ; Ahmad, Arshia Q; Sreekantan-Nair, Ajith; Weedon, Michael N; Rich, Phil; Patton, Michael A; Warner, Thomas T; Silver, David L; Crosby, Andrew H
	1-Dec-2018	Homozygous mutation in MFSD2A, encoding a lysolipid transporter for docosahexanoic acid, is associated with microcephaly and hypomyelination	Harel, Tamar; Quek, Debra QY; Wong, Bernice H; Cazenave-Gassiot, Amaury; Wenk, Markus R ; Fan, Hao ; Berger, Itai; Shmueli, Dorit; Shaag, Avraham; Silver, David L; Elpeleg, Orly; Edvardson, Shimon
	1-Jul-2015	Inactivating mutations in MFSD2A, required for omega-3 fatty acid transport in brain, cause a lethal microcephaly syndrome	Guemez-Gamboa, Alicia; Nguyen, Long N; Yang, Hongbo; Zaki, Maha S; Kara, Majdi; Ben-Omran, Tawfeg; Akizu, Naiara; Rosti, Rasim Ozgur; Rosti, Basak; Scott, Eric; Schroth, Jana; Copeland, Brett; Vaux, Keith K; Cazenave-Gassiot, Amaury ; Quek, Debra QY; Wong, Bernice H ; Tan, Bryan C; Wenk, Markus R ; Gunel, Murat; Gabriel, Stacey; Chi, Neil C; Silver, David L ; Gleeson, Joseph G

Showing results 1 to 3 of 3