Familial idiopathic methaemoglobinaemia, associated with mental deficiency and neurological abnormalities.
about
Exonic point mutations in NADH-cytochrome B5 reductase genes of homozygotes for hereditary methemoglobinemia, types I and III: putative mechanisms of tissue-dependent enzyme deficiencyMethemoglobinemiaDiscussion on some clinical, genetic and biochemical aspects of metabolic disorders of the nervous system: metabolic disease of the nervous system: clinical aspectsThe widening etiology of mental defect.
P2860
Familial idiopathic methaemoglobinaemia, associated with mental deficiency and neurological abnormalities.
description
1953 nî lūn-bûn
@nan
1953年の論文
@ja
1953年学术文章
@wuu
1953年学术文章
@zh
1953年学术文章
@zh-cn
1953年学术文章
@zh-hans
1953年学术文章
@zh-my
1953年学术文章
@zh-sg
1953年學術文章
@yue
1953年學術文章
@zh-hant
name
Familial idiopathic methaemogl ...... nd neurological abnormalities.
@en
Familial idiopathic methaemogl ...... nd neurological abnormalities.
@nl
type
label
Familial idiopathic methaemogl ...... nd neurological abnormalities.
@en
Familial idiopathic methaemogl ...... nd neurological abnormalities.
@nl
prefLabel
Familial idiopathic methaemogl ...... nd neurological abnormalities.
@en
Familial idiopathic methaemogl ...... nd neurological abnormalities.
@nl
P2093
P2860
P356
P1433
P1476
Familial idiopathic methaemogl ...... nd neurological abnormalities.
@en
P2093
WORSTER-DROUGHT C
P2860
P304
P356
10.1136/BMJ.2.4828.114
P407
P577
1953-07-01T00:00:00Z