(Q41981517)

14 October 2017

title

Neonatal form of the hyperornithinaemia, hyperammonaemia, and homocitrullinuria (HHH) syndrome and prenatal diagnosis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1438066

ornithine carbamoyltransferase deficiency

26 September 2022

main subject

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1438066

26 September 2022

author name string

V. E. Shih

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1438066

26 September 2022

R. Laframboise

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1438066

26 September 2022

R. Mandell

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1438066

26 September 2022

J. Pichette

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1438066

26 September 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1438066

26 September 2022

publication date

1 September 1992

1 reference

14 October 2017

1 reference

14 October 2017

volume

12

1 reference

14 October 2017

issue

9

1 reference

14 October 2017

page(s)

717-723

1 reference

Ornithinemia, hyperammonemia, and homocitrullinuria. A disease associated with mental retardation and possibly caused by defective mitochondrial transport

14 October 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FPD.1970120905

21 January 2018

Identifiers

DOI

10.1002/PD.1970120905

1 reference

14 October 2017

1 reference