DOI: 10.1055/s-00000034

Klinische Pädiatrie

References

Mitchell  GA, Ozand  PT, Robert  M-F et al.
HMG-CoA Lyase Deficiency: Identification of five causal point mutations in codons 41 and 42, including a frequent Saudi Arabian mutation, R41Q. 
Am J Hum Genet 1998; 62: 295-300  

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