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Quek, Debra QY
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Showing results 1 to 3 of 3
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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