Results
|
|
1.
|
|
|
|
2.
|
|
|
|
3.
|
Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: clinical course and description of causal mutations in two patients. [electronic resource] by
- Bouchard, L
- Robert, M F
- Vinarov, D
- Stanley, C A
- Thompson, G N
- Morris, A
- Leonard, J V
- Quant, P
- Hsu, B Y
- Boneh, A
- Boukaftane, Y
- Ashmarina, L
- Wang, S
- Miziorko, H
- Mitchell, G A
Producer: 20010712
In:
Pediatric research vol. 49
Availability: No items available.
|
|
|
4.
|
|
|
|
5.
|
|
|
|
6.
|
|
|
|
7.
|
|
|
|
8.
|
|
|
|
9.
|
|
|
|
10.
|
|
|
|
11.
|
|
|
|
12.
|
|
|
|
13.
|
|
|
|
14.
|
|
|
|
15.
|
|
|
|
16.
|
A 3-hydroxy-3-methylglutaryl-CoA synthase-based probe for the discovery of the acyltransferase-less type I polyketide synthases. [electronic resource] by
- Liang, Haoyu
- Jiang, Lin
- Jiang, Qiyun
- Shi, Jie
- Xiang, Jingxi
- Yan, Xiaohui
- Zhu, Xiangcheng
- Zhao, Lixing
- Shen, Ben
- Duan, Yanwen
- Huang, Yong
Producer: 20200505
In:
Environmental microbiology vol. 21
Availability: No items available.
|
|
|
17.
|
|
|
|
18.
|
|
|
|
19.
|
|
|
|
20.
|
|