HYDROXYKYNURENINURIA: A CASE OF ABNORMAL TRYPTOPHAN METABOLISM PROBABLY DUE TO A DEFICIENCY OF KYNURENINASE
about
The screening of hereditary metabolic defects among newborn infantsMetabolism of tryptophan in childhood epilepsySevere intellectual disability, omphalocele, hypospadia and high blood pressure associated to a deletion at 2q22.1q22.3: case report.Aspects of tryptophan metabolism in health and disease: a review.Possible roles of excess tryptophan metabolites in cancer.A disorder of tryptophan metabolism in chronic granulomatous diseaseOrganic acidurias and related abnormalities.
P2860
Q35917960-6A5F089D-B7EF-4A08-ABAF-7129B01A3020Q36061319-7C4399E9-85C5-4DAC-ADE3-4C9149FB61B6Q36125601-2A11AAB9-803D-48FB-9C4E-420339CCFCADQ36633569-505A753C-96B7-4C39-ACA5-EDBDE960D3DCQ37788635-A401F3C3-2E1A-4AD3-9F78-1F18E23FB1C6Q39495658-C6374F3F-F4BC-4E05-A292-8FB86DCBEF68Q40422979-A4A5ED21-0AFC-402E-89D1-98712DF644E8
P2860
HYDROXYKYNURENINURIA: A CASE OF ABNORMAL TRYPTOPHAN METABOLISM PROBABLY DUE TO A DEFICIENCY OF KYNURENINASE
description
1964 nî lūn-bûn
@nan
1964年の論文
@ja
1964年論文
@yue
1964年論文
@zh-hant
1964年論文
@zh-hk
1964年論文
@zh-mo
1964年論文
@zh-tw
1964年论文
@wuu
1964年论文
@zh
1964年论文
@zh-cn
name
HYDROXYKYNURENINURIA: A CASE O ...... O A DEFICIENCY OF KYNURENINASE
@ast
HYDROXYKYNURENINURIA: A CASE O ...... O A DEFICIENCY OF KYNURENINASE
@en
type
label
HYDROXYKYNURENINURIA: A CASE O ...... O A DEFICIENCY OF KYNURENINASE
@ast
HYDROXYKYNURENINURIA: A CASE O ...... O A DEFICIENCY OF KYNURENINASE
@en
prefLabel
HYDROXYKYNURENINURIA: A CASE O ...... O A DEFICIENCY OF KYNURENINASE
@ast
HYDROXYKYNURENINURIA: A CASE O ...... O A DEFICIENCY OF KYNURENINASE
@en
P2093
P2860
P356
P1476
HYDROXYKYNURENINURIA: A CASE O ...... O A DEFICIENCY OF KYNURENINASE
@en
P2093
G M KOMROWER
R G WESTALL
P2860
P304
P356
10.1136/ADC.39.205.250
P407
P577
1964-06-01T00:00:00Z