Treatment of X-linked creatine transporter (SLC6A8) deficiency: systematic review of the literature and three new cases.
about
Genes with high penetrance for syndromic and non-syndromic autism typically function within the nucleus and regulate gene expression.Diagnostic methods and recommendations for the cerebral creatine deficiency syndromes.In Vivo NMR Studies of the Brain with Hereditary or Acquired Metabolic Disorders.Epileptic Encephalopathy in Childhood: A Stepwise Approach for Identification of Underlying Genetic Causes.Treatable Genetic Metabolic Epilepsies.Creatine transporter deficiency leads to increased whole body and cellular metabolism.
P2860
Treatment of X-linked creatine transporter (SLC6A8) deficiency: systematic review of the literature and three new cases.
description
2014 nî lūn-bûn
@nan
2014 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Treatment of X-linked creatine ...... iterature and three new cases.
@ast
Treatment of X-linked creatine ...... iterature and three new cases.
@en
type
label
Treatment of X-linked creatine ...... iterature and three new cases.
@ast
Treatment of X-linked creatine ...... iterature and three new cases.
@en
prefLabel
Treatment of X-linked creatine ...... iterature and three new cases.
@ast
Treatment of X-linked creatine ...... iterature and three new cases.
@en
P2093
P31
P1476
Treatment of X-linked creatine ...... iterature and three new cases.
@en
P2093
Clara D M van Karnebeek
Mary Dunbar
Michael Sargent
Sravan Jaggumantri
P304
P356
10.1016/J.YMGME.2014.05.011
P577
2014-05-29T00:00:00Z