000 01423 a2200349 4500
005 20250517101908.0
264 0 _c20180103
008 201801s 0 0 eng d
022 _a1872-9754
024 7 _a10.1016/j.neuint.2016.06.009
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMalaspina, P
245 0 0 _aSuccinic semialdehyde dehydrogenase deficiency (SSADHD): Pathophysiological complexity and multifactorial trait associations in a rare monogenic disorder of GABA metabolism.
_h[electronic resource]
260 _bNeurochemistry international
_c10 2016
300 _a72-84 p.
_bdigital
500 _aPublication Type: Journal Article; Review; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
650 0 4 _aAmino Acid Metabolism, Inborn Errors
_xgenetics
650 0 4 _aAnimals
650 0 4 _aDevelopmental Disabilities
_xgenetics
650 0 4 _aGenetic Association Studies
_xmethods
650 0 4 _aHumans
650 0 4 _aMultifactorial Inheritance
_xphysiology
650 0 4 _aSuccinate-Semialdehyde Dehydrogenase
_xdeficiency
650 0 4 _agamma-Aminobutyric Acid
_xmetabolism
700 1 _aRoullet, J-B
700 1 _aPearl, P L
700 1 _aAinslie, G R
700 1 _aVogel, K R
700 1 _aGibson, K M
773 0 _tNeurochemistry international
_gvol. 99
_gp. 72-84
856 4 0 _uhttps://doi.org/10.1016/j.neuint.2016.06.009
_zAvailable from publisher's website
999 _c26131894
_d26131894