000 01348 a2200421 4500
005 20250512235558.0
264 0 _c19830909
008 198309s 0 0 eng d
022 _a0022-3476
024 7 _a10.1016/s0022-3476(83)80351-5
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aWolf, B
245 0 0 _aPhenotypic variation in biotinidase deficiency.
_h[electronic resource]
260 _bThe Journal of pediatrics
_cAug 1983
300 _a233-7 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aAmidohydrolases
_xdeficiency
650 0 4 _aBiotin
_xmetabolism
650 0 4 _aBiotinidase
650 0 4 _aCarboxy-Lyases
_xdeficiency
650 0 4 _aChild, Preschool
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aInfant, Newborn
650 0 4 _aMale
650 0 4 _aNeurologic Manifestations
650 0 4 _aSkin Manifestations
700 1 _aGrier, R E
700 1 _aAllen, R J
700 1 _aGoodman, S I
700 1 _aKien, C L
700 1 _aParker, W D
700 1 _aHowell, D M
700 1 _aHurst, D L
773 0 _tThe Journal of pediatrics
_gvol. 103
_gno. 2
_gp. 233-7
856 4 0 _uhttps://doi.org/10.1016/s0022-3476(83)80351-5
_zAvailable from publisher's website
999 _c6875444
_d6875444