<i>Nhlrc2</i> is crucial during mouse gastrulation-Reference-Cited by-同舟云学术

Nhlrc2 is crucial during mouse gastrulation

Published:2022-03 Issue:3 Volume:60 Page:
ISSN:1526-954X
Container-title:genesis
language:en
Short-container-title:Genesis

Author:

Hiltunen Anniina E.¹^ORCID,Vuolteenaho Reetta²,Ronkainen Veli‐Pekka²,Miinalainen Ilkka²,Uusimaa Johanna¹³,Lehtonen Siri¹⁴,Hinttala Reetta¹²^ORCID

Affiliation:

1. Medical Research Center Oulu and PEDEGO Research Unit University of Oulu and Oulu University Hospital Oulu Finland

2. Biocenter Oulu University of Oulu Oulu Finland

3. Clinic for Children and Adolescents Pediatric Neurology Unit, Oulu University Hospital Oulu Finland

4. Department of Obstetrics and Gynecology Oulu University Hospital Oulu Finland

Funder

Academy of Finland

Lastentautien Tutkimussäätiö

Publisher

Wiley

Subject

Cell Biology,Endocrinology,Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/dvg.23470

Reference35 articles.

1. Structural analysis of human NHLRC2, mutations of which are associated with FINCA disease

2. Novel compound heterozygous variants in NHLRC2 in a patient with FINCA syndrome

3. Delhotal J. D. J.(2016). Characterization of NHLRC2 gene‐edited mice: a model for bovine developmental duplications. Retrieved fromhttps://www.ideals.illinois.edu/handle/2142/92824

4. Genotype disclosure in the genomics era: roles and responsibilities

5. Identification of phagocytosis regulators using magnetic genome-wide CRISPR screens

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4. Broadening the phenotypic and molecular spectrum of FINCA syndrome: Biallelic NHLRC2 variants in 15 novel individuals;European Journal of Human Genetics;2023-05-15

5. Novel patients with NHLRC2 variants expand the phenotypic spectrum of FINCA disease;Frontiers in Neuroscience;2023-04-27