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4781.
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4782.
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4783.
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Clinical and biochemical characterization of four patients with mutations in ECHS1. [electronic resource] by
- Ferdinandusse, Sacha
- Friederich, Marisa W
- Burlina, Alberto
- Ruiter, Jos P N
- Coughlin, Curtis R
- Dishop, Megan K
- Gallagher, Renata C
- Bedoyan, Jirair K
- Vaz, Frédéric M
- Waterham, Hans R
- Gowan, Katherine
- Chatfield, Kathryn
- Bloom, Kaitlyn
- Bennett, Michael J
- Elpeleg, Orly
- Van Hove, Johan L K
- Wanders, Ronald J A
Producer: 20160229
In:
Orphanet journal of rare diseases vol. 10
Availability: No items available.
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4784.
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4785.
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4786.
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4787.
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4788.
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4789.
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4790.
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4791.
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4792.
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4793.
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4794.
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4795.
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4796.
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Tissue-Specific Ablation of ACSL4 Results in Disturbed Steroidogenesis. [electronic resource] by
- Wang, Wei
- Hao, Xiao
- Han, Lina
- Yan, Zhe
- Shen, Wen-Jun
- Dong, Dachuan
- Hasbargen, Kathrin
- Bittner, Stefanie
- Cortez, Yuan
- Greenberg, Andrew S
- Azhar, Salman
- Kraemer, Fredric B
Producer: 20191223
In:
Endocrinology vol. 160
Availability: No items available.
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4797.
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Probing the Flexibility of an Iterative Modular Polyketide Synthase with Non-Native Substrates in Vitro. [electronic resource] by
- Curran, Samuel C
- Hagen, Andrew
- Poust, Sean
- Chan, Leanne Jade G
- Garabedian, Brett M
- de Rond, Tristan
- Baluyot, Marian-Joy
- Vu, Jonathan T
- Lau, Andrew K
- Yuzawa, Satoshi
- Petzold, Christopher J
- Katz, Leonard
- Keasling, Jay D
Producer: 20190313
In:
ACS chemical biology vol. 13
Availability: No items available.
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4798.
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A case report of a mild form of multiple acyl-CoA dehydrogenase deficiency due to compound heterozygous mutations in the ETFA gene. [electronic resource] by
- Chautard, Robin
- Laroche-Raynaud, Cécile
- Lia, Anne-Sophie
- Chazelas, Pauline
- Derouault, Paco
- Sturtz, Franck
- Baaj, Yasser
- Veauville-Merllié, Alice
- Acquaviva, Cécile
- Favreau, Frédéric
- Faye, Pierre-Antoine
Producer: 20201216
In:
BMC medical genomics vol. 13
Availability: No items available.
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4799.
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4800.
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