Haploinsufficiency as a disease mechanism in GNB1 ‐associated neurodevelopmental disorder-Reference-Cited by-同舟云学术

Haploinsufficiency as a disease mechanism in GNB1 ‐associated neurodevelopmental disorder

Published:2020-09-12 Issue:11 Volume:8 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Schultz‐Rogers Laura¹^ORCID,Masuho Ikuo²,Pinto e Vairo Filippo¹³,Schmitz Christopher T.⁴,Schwab Tanya L.⁴,Clark Karl J.⁴,Gunderson Lauren³,Pichurin Pavel N.³,Wierenga Klaas⁵,Martemyanov Kirill A.²,Klee Eric W.¹³^ORCID

Affiliation:

1. Center for Individualized Medicine Mayo Clinic Rochester MN USA

2. Department of Neuroscience The Scripps Research Institute Jupiter FL USA

3. Department of Clinical Genomics Mayo Clinic Rochester MN USA

4. Department of Biochemistry and Molecular Biology Mayo Clinic Rochester MN USA

5. Department of Medical Genetics Mayo Clinic Jacksonville FL USA

Funder

Foundation for the National Institutes of Health

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1477

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5. DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

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