000 01059 a2200325 4500
005 20250512090556.0
264 0 _c19711005
008 197110s 0 0 eng d
022 _a0140-6736
024 7 _a10.1016/s0140-6736(71)91822-8
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBlass, J P
245 0 0 _aIntermittent ataxia with pyruvate-decarboxylase deficiency.
_h[electronic resource]
260 _bLancet (London, England)
_cJun 1971
300 _a1302 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAlanine
_xurine
650 0 4 _aAtaxia
_xcomplications
650 0 4 _aCarboxy-Lyases
650 0 4 _aHartnup Disease
_xmetabolism
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMetabolism, Inborn Errors
_xcomplications
650 0 4 _aPyruvates
_xblood
700 1 _aLonsdale, D
700 1 _aUhlendorf, B W
700 1 _aHom, E
773 0 _tLancet (London, England)
_gvol. 1
_gno. 7712
_gp. 1302
856 4 0 _uhttps://doi.org/10.1016/s0140-6736(71)91822-8
_zAvailable from publisher's website
999 _c4110412
_d4110412