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Author/Creator Latta, Femke

3. Long-Read Sequencing Identifies Novel Pathogenic Intronic Variants in Gitelman Syndrome. Issue 2 (9th February 2023)

Authors:
Viering, Daan H.H.M.; Hureaux, Marguerite; Neveling, Kornelia; Latta, Femke; Kwint, Michael; Blanchard, Anne; Konrad, Martin; Bindels, René J.M.; Schlingmann, Karl-Peter; Vargas-Poussou, Rosa; de Baaij, Jeroen H.F.
Journal:
Journal of the American Society of Nephrology
Issue:
Volume 34:Issue 2(2023)
Page Start:
333
Record Type:
Journal Article
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4. Possible role for rare TRPM7 variants in patients with hypomagnesaemia with secondary hypocalcaemia. Issue 3 (13th May 2022)

Authors:
Vargas-Poussou, Rosa; Claverie-Martin, Felix; Prot-Bertoye, Caroline; Carotti, Valentina; van der Wijst, Jenny; Perdomo-Ramirez, Ana; Fraga-Rodriguez, Gloria M; Hureaux, Marguerite; Bos, Caro; Latta, Femke; Houillier, Pascal; Hoenderop, Joost G J; de Baaij, Jeroen H F
Journal:
Nephrology dialysis transplantation
Issue:
Volume 38:Issue 3(2023)
Page Start:
679
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

5. The phenotypic and genetic spectrum of patients with heterozygous mutations in cyclin M2 (CNNM2). Issue 4 (1st March 2021)

Authors:
Franken, Gijs A. C.; Müller, Dominik; Mignot, Cyril; Keren, Boris; Lévy, Jonathan; Tabet, Anne‐Claude; Germanaud, David; Tejada, María‐Isabel; Kroes, Hester Y.; Nievelstein, Rutger A. J.; Brimble, Elise; Ruzhnikov, Maria; Claverie‐Martin, Felix; Szczepańska, Maria; Ćuk, Martin; Latta, Femke; Konr...
Journal:
Human mutation
Issue:
Volume 42:Issue 4(2021)
Page Start:
473
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗