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25541.
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25542.
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25543.
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25544.
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How chromosomal deletions can unmask recessive mutations? Deletions in 10q11.2 associated with CHAT or SLC18A3 mutations lead to congenital myasthenic syndrome. [electronic resource] by
- Schwartz, Mathias
- Sternberg, Damien
- Whalen, Sandra
- Afenjar, Alexandra
- Isapof, Arnaud
- Chabrol, Brigitte
- Portnoï, Marie-France
- Heide, Solveig
- Keren, Boris
- Chantot-Bastaraud, Sandra
- Siffroi, Jean-Pierre
Producer: 20180621
In:
American journal of medical genetics. Part A vol. 176
Availability: No items available.
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25545.
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25546.
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25547.
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Nonalcoholic fatty liver disease alters microcystin-LR toxicokinetics and acute toxicity. [electronic resource] by
- Clarke, John D
- Dzierlenga, Anika
- Arman, Tarana
- Toth, Erica
- Li, Hui
- Lynch, Katherine D
- Tian, Dan-Dan
- Goedken, Michael
- Paine, Mary F
- Cherrington, Nathan
Producer: 20190624
In:
Toxicon : official journal of the International Society on Toxinology vol. 162
Availability: No items available.
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25548.
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25549.
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25550.
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25560.
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