(Q55670918)

English

Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: clinical course and description of causal mutations in two patients

article

Statements

Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: clinical course and description of causal mutations in two patients (English)
0 references
L Bouchard
0 references
M F Robert
0 references
D Vinarov
0 references
C A Stanley
0 references
G N Thompson
0 references
A Morris
0 references
J V Leonard
0 references
P Quant
0 references
B Y Hsu
0 references
A Boneh
0 references
Y Boukaftane
0 references
L Ashmarina
0 references
S Wang
0 references
H Miziorko
0 references
G A Mitchell
0 references
March 2001
0 references
49
0 references
3
0 references
326-31
0 references

Identifiers

 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit