A Common X-Linked Inborn Error of Carnitine Biosynthesis May Be a Risk Factor for Non-Dysmorphic Autism

AuthID
P-002-CHF
36
Author(s)
Crawford, EL
·
Luo, R
·
Lionel, AC
·
Cai, GQ
·
Sadikovic, B
·
Lee, K
·
Lo, C
·
[+16]·
Geschwind, D
·
Sutcliffe, JS
·
Hurles, ME
·
Wanders, RJA
·
Shaw, CA
·
Leal, SM
·
Cook, EH
·
Goin Kochel, RP
·
Vaz, FM
·
Beaudet, AL
Document Type
Abstract
Year published
2012
Published
in MOLECULAR GENETICS AND METABOLISM, ISSN: 1096-7192
Volume: 105, Issue: 3, Pages: 308-309 (2)
Conference
35Th Annual Meeting of the Society-For-Inherited-Metabolic-Disorders (Simd), Date: MAR 31-APR 03, 2012, Location: Charlotte, NC, Sponsors: Soc Inherited Metabol Disorders (SIMD), Abbott Nutr (Abbott Metabol), Pfizer Inc, Shire, Actel Pharmaceut (ACTELION), Cytonet LLC, GeneDx, Genzyme, Hyper Therapeut, Inc, Mead Johnson Nutr, Orphan Europe Recordati Grp, Rare Dis Therapeut, Inc, Ucyclyd Pharma, Vitaflo, Appl Nutr Corp, ARUP Labs, BioMarin Pharmaceut, Inc, Cambrooke Foods, Inc, Emory Genet Lab, Hitachi High Technol Amer, Inc, Prevent Genet, Transgenom, Inc, Canadian PKU & Allied Disorders Inc, Natl PKU Alliance, Natl Urea Cycle Disorders Fdn, Propion Acidemia Fdn, United Mitochondrial Dis Fdn
Indexing
Publication Identifiers
Wos: WOS:000301906400051
Source Identifiers
ISSN: 1096-7192
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Name Order Name   Name Order Name   Name Order Name
1 Celestino Soper, PBS;   2 Violante, S;   3 Crawford, EL;
4 Luo, R;   5 Lionel, AC;   6 Delaby, E;
7 Cai, GQ;   8 Sadikovic, B;   9 Lee, K;
10 Lo, C;   11 Gao, K;   12 Person, RE;
13 Moss, TJ;   14 German, JR;   15 Huang, N;
16 Shinawi, M;   17 Treadwell Deering, D;   18 Szatmari, P;
19 Roberts, W;   20 Fernandez, B;   21 Schroer, RJ;
22 Stevenson, RE;   23 Buxbaum, JD;   24 Betancur, C;
25 Scherer, SW;   26 Sanders, SJ;   27 Geschwind, D;
28 Sutcliffe, JS;   29 Hurles, ME;   30 Wanders, RJA;
31 Shaw, CA;   32 Leal, SM;   33 Cook, EH;
34 Goin Kochel, RP;   35 Vaz, FM;   36 Beaudet, AL;