Wikidata

(Q42662095)

English

3-Methylcrotonyl-CoA carboxylase deficiency: mutation analysis in 28 probands, 9 symptomatic and 19 detected by newborn screening

scientific article published on August 2005

In more languages

Statements

title
3-Methylcrotonyl-CoA carboxylase deficiency: mutation analysis in 28 probands, 9 symptomatic and 19 detected by newborn screening (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
16010683
retrieved
4 November 2017
author name string
Maria Fernanda Dantas
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
16010683
retrieved
4 November 2017
Terttu Suormala
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
16010683
retrieved
4 November 2017
Ann Randolph
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
16010683
retrieved
4 November 2017
David Coelho
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
16010683
retrieved
4 November 2017
Brian Fowler
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
16010683
retrieved
4 November 2017
David Valle
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed ID
16010683
retrieved
4 November 2017
publication date
1 August 2005
1 reference
stated in
Europe PubMed Central
PubMed ID
16010683
retrieved
4 November 2017

Identifiers

 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit
                    Retrieved from "https://www.wikidata.org/w/index.php?title=Q42662095&oldid=1964947367"