Case Report of a Juvenile Patient with Autism Spectrum Disorder with a Novel Combination of Copy Number Variants in <i>ADGRL3</i> (<i>LPHN3</i>) and Two Pseudogenes.
- DOI
- 10.2147/tacg.s361239
- Published
- 2022-09-02
- Container
- Appl Clin Genet
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.2147/tacg.s361239,
title = {Case Report of a Juvenile Patient with Autism Spectrum Disorder with a Novel Combination of Copy Number Variants in <i>ADGRL3</i> (<i>LPHN3</i>) and Two Pseudogenes.},
author = {Maurer MH and Kohler A and Hudemann M and Jüngling J and Biskup S and Menzel M.},
year = {2022},
journal = {Appl Clin Genet},
doi = {10.2147/tacg.s361239},
url = {https://doi.org/10.2147/tacg.s361239}
}RIS
TY - JOUR TI - Case Report of a Juvenile Patient with Autism Spectrum Disorder with a Novel Combination of Copy Number Variants in <i>ADGRL3</i> (<i>LPHN3</i>) and Two Pseudogenes. AU - Maurer MH AU - Kohler A AU - Hudemann M AU - Jüngling J AU - Biskup S AU - Menzel M. PY - 2022 JO - Appl Clin Genet DO - 10.2147/tacg.s361239 UR - https://doi.org/10.2147/tacg.s361239 ER -
APA
MH, M., A, K., M, H., J, J., S, B., & M., M. (2022). Case Report of a Juvenile Patient with Autism Spectrum Disorder with a Novel Combination of Copy Number Variants in <i>ADGRL3</i> (<i>LPHN3</i>) and Two Pseudogenes.. Appl Clin Genet. https://doi.org/10.2147/tacg.s361239
Source records
- europe-pmc · retrieved 2026-09-27T13:34:31.074Z