(Q24298532)

English

Genetic polymorphism of human cytochrome P-450 (S)-mephenytoin 4-hydroxylase. Studies with human autoantibodies suggest a functionally altered cytochrome P-450 isozyme as cause of the genetic deficiency

scientific article

In more languages

edit

Statements

instance of

scholarly article

0 references

title

Genetic polymorphism of human cytochrome P-450 (S)-mephenytoin 4-hydroxylase. Studies with human autoantibodies suggest a functionally altered cytochrome P-450 isozyme as cause of the genetic deficiency (English)

0 references

main subject

cytochrome P450 family 2 subfamily C member 19

1 reference

stated in

GOA release 2020-03-11

oxygen binding

1 reference

stated in

GOA release 2020-03-11

1 reference

U T Meier

1

0 references

U A Meyer

series ordinal

2

0 references

language of work or name

English

0 references

publication date

15 December 1987

0 references

published in

Biochemistry

0 references

volume

26

0 references

page(s)

8466-74

0 references

issue

25

0 references

Identifiers

0 references

0 references

(Q24298532)

Genetic polymorphism of human cytochrome P-450 (S)-mephenytoin 4-hydroxylase. Studies with human autoantibodies suggest a functionally altered cytochrome P-450 isozyme as cause of the genetic deficiency

Statements

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)