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Author/Creator Dupas, Quentin

1. Identification of a novel splice site mutation in the SERAC1 gene responsible for the MEGDHEL syndrome. Issue 8 (28th June 2019)

Authors:
Snanoudj, Sarah; Mordel, Patrick; Dupas, Quentin; Schanen, Cécile; Arion, Alina; Gérard, Marion; Read, Marie‐Hélène; Nait Rabah, Djamel; Goux, Didier; Chapon, Françoise; Jokic, Mickael; Allouche, Stéphane
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 7:Issue 8(2019)
Page Start:
n/a
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Identification of a novel splice site mutation in the SERAC1 gene responsible for the MEGDHEL syndrome1. Issue 8 (28th June 2019)

Authors:
Snanoudj, Sarah; Mordel, Patrick; Dupas, Quentin; Schanen, Cécile; Arion, Alina; Gérard, Marion; Read, Marie‐Hélène; Nait Rabah, Djamel; Goux, Didier; Chapon, Françoise; Jokic, Mickael; Allouche, Stéphane
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 7:Issue 8(2019)
Page Start:
n/a
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Impact of T161, Y318 and S363 alanine mutations on regulation of the human delta-opioid receptor (hDOPr) induced by peptidic and alkaloid agonists. (15th November 2020)

Authors:
Camacho, Elise; Marie, Nicolas; Dupas, Quentin; Martel, Caroline; Nowoczyn, Marie; Elie, Nicolas; Rochais, Christophe; Töth, Geza; Allouche, Stéphane
Journal:
Neuropharmacology
Issue:
Volume 179(2020)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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