Mutations inSLC1A4, encoding the brain serine transporter, are associated with developmental delay, microcephaly and hypomyelination-Reference-Cited by-同舟云学术

Mutations inSLC1A4, encoding the brain serine transporter, are associated with developmental delay, microcephaly and hypomyelination

Published:2015-06-03 Issue:8 Volume:52 Page:541-547
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:J Med Genet

Author:

Damseh Nadirah,Simonin Alexandre,Jalas Chaim,Picoraro Joseph A,Shaag Avraham,Cho Megan T,Yaacov Barak,Neidich Julie,Al-Ashhab Motee,Juusola Jane,Bale Sherri,Telegrafi Aida,Retterer Kyle,Pappas John G,Moran Ellen,Cappell Joshua,Anyane Yeboa Kwame,Abu-Libdeh Bassam,Hediger Matthias A,Chung Wendy K,Elpeleg Orly,Edvardson Simon

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference14 articles.

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5. Functional identification of ASCT1 neutral amino acid transporter as the predominant system for the uptake of L-serine in rat neurons in primary culture;Yamamoto;Neurosci Res,2004

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