Wikidata

(Q28296731)

English

The neurogenic weakness, ataxia and retinitis pigmentosa (NARP) syndrome mtDNA mutation (T8993G) triggers muscle ATPase deficiency and hypocitrullinaemia

scientific article

In more languages

Statements

title
The neurogenic weakness, ataxia and retinitis pigmentosa (NARP) syndrome mtDNA mutation (T8993G) triggers muscle ATPase deficiency and hypocitrullinaemia (English)
0 references
author name string
B Parfait
series ordinal
1
0 references
P de Lonlay
series ordinal
2
0 references
J C von Kleist-Retzow
series ordinal
3
0 references
V Cormier-Daire
series ordinal
4
0 references
D Chrétien
series ordinal
5
0 references
A Rötig
series ordinal
6
0 references
D Rabier
series ordinal
7
0 references
J M Saudubray
series ordinal
8
0 references
P Rustin
series ordinal
9
0 references
publication date
January 1999
0 references
volume
158
0 references
issue
1
0 references
page(s)
55-8
0 references

Identifiers

DOI
10.1007/S004310051009
0 references
 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit
                    Retrieved from "https://www.wikidata.org/w/index.php?title=Q28296731&oldid=2175218393"