000 01485 a2200469 4500
005 20250512121646.0
264 0 _c19730130
008 197301s 0 0 eng d
022 _a0028-4793
024 7 _a10.1056/NEJM197301042880102
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aShort, E M
245 0 0 _aEvidence for x-linked dominant inheritance of ornithine transcarbamylase deficiency.
_h[electronic resource]
260 _bThe New England journal of medicine
_cJan 1973
300 _a7-12 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAdult
650 0 4 _aAmino Acid Metabolism, Inborn Errors
_xdiagnosis
650 0 4 _aAmmonia
_xblood
650 0 4 _aBiopsy, Needle
650 0 4 _aDiet Therapy
650 0 4 _aDietary Proteins
650 0 4 _aFemale
650 0 4 _aGenes, Dominant
650 0 4 _aHeterozygote
650 0 4 _aHumans
650 0 4 _aInfant, Newborn
650 0 4 _aInfant, Newborn, Diseases
_xdiagnosis
650 0 4 _aLiver
_xenzymology
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aOrnithine Carbamoyltransferase
_xmetabolism
650 0 4 _aPedigree
650 0 4 _aSex Chromosomes
650 0 4 _aSex Factors
700 1 _aConn, H O
700 1 _aSnodgrass, P J
700 1 _aCampbell, A G
700 1 _aRosenberg, L E
773 0 _tThe New England journal of medicine
_gvol. 288
_gno. 1
_gp. 7-12
856 4 0 _uhttps://doi.org/10.1056/NEJM197301042880102
_zAvailable from publisher's website
999 _c4685596
_d4685596