Results
|
|
19441.
|
|
|
|
19442.
|
|
|
|
19443.
|
|
|
|
19444.
|
|
|
|
19445.
|
HMG CoA lyase deficiency: identification of five causal point mutations in codons 41 and 42, including a frequent Saudi Arabian mutation, R41Q. [electronic resource] by
- Mitchell, G A
- Ozand, P T
- Robert, M F
- Ashmarina, L
- Roberts, J
- Gibson, K M
- Wanders, R J
- Wang, S
- Chevalier, I
- Plöchl, E
- Miziorko, H
Producer: 19980406
In:
American journal of human genetics vol. 62
Availability: No items available.
|
|
|
19446.
|
|
|
|
19447.
|
|
|
|
19448.
|
|
|
|
19449.
|
|
|
|
19450.
|
|
|
|
19451.
|
|
|
|
19452.
|
|
|
|
19453.
|
|
|
|
19454.
|
|
|
|
19455.
|
|
|
|
19456.
|
|
|
|
19457.
|
|
|
|
19458.
|
|
|
|
19459.
|
|
|
|
19460.
|
|