Heterozygous Variants in LRP1 Cause a Neurodevelopmental Disorder With Congenital Heart Defects.

Rippert AL, Arnadottir GA, Bedinger L, Brunetti-Pierri N, Cech J, Chen X, Chen Y, Chick E, Dyack S, Franchi M, Frey T, Genevieve D, Glass I, Granadillo J, Keener KA, MacKay SB, McDunnah P, Misra VK, Monaghan KG, Mullegama SV, Peduto C, Peterman-Prather L, Rauch A, Somerville C, Stefansson K, Steindl K, Sulem P, Sulem T, Trapane P, Zeuli R, Zinner S, Izumi K

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DOI: 10.1002/ajmg.a.70261
Published: 2026 Aug 26
Container: American journal of medical genetics. Part A
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1002/ajmg.a.70261,
  title = {Heterozygous Variants in LRP1 Cause a Neurodevelopmental Disorder With Congenital Heart Defects.},
  author = {Rippert AL and Arnadottir GA and Bedinger L and Brunetti-Pierri N and Cech J and Chen X and Chen Y and Chick E and Dyack S and Franchi M and Frey T and Genevieve D and Glass I and Granadillo J and Keener KA and MacKay SB and McDunnah P and Misra VK and Monaghan KG and Mullegama SV and Peduto C and Peterman-Prather L and Rauch A and Somerville C and Stefansson K and Steindl K and Sulem P and Sulem T and Trapane P and Zeuli R and Zinner S and Izumi K},
  year = {2026},
  journal = {American journal of medical genetics. Part A},
  doi = {10.1002/ajmg.a.70261},
  url = {https://doi.org/10.1002/ajmg.a.70261}
}

RIS

TY  - JOUR
TI  - Heterozygous Variants in LRP1 Cause a Neurodevelopmental Disorder With Congenital Heart Defects.
AU  - Rippert AL
AU  - Arnadottir GA
AU  - Bedinger L
AU  - Brunetti-Pierri N
AU  - Cech J
AU  - Chen X
AU  - Chen Y
AU  - Chick E
AU  - Dyack S
AU  - Franchi M
AU  - Frey T
AU  - Genevieve D
AU  - Glass I
AU  - Granadillo J
AU  - Keener KA
AU  - MacKay SB
AU  - McDunnah P
AU  - Misra VK
AU  - Monaghan KG
AU  - Mullegama SV
AU  - Peduto C
AU  - Peterman-Prather L
AU  - Rauch A
AU  - Somerville C
AU  - Stefansson K
AU  - Steindl K
AU  - Sulem P
AU  - Sulem T
AU  - Trapane P
AU  - Zeuli R
AU  - Zinner S
AU  - Izumi K
PY  - 2026
JO  - American journal of medical genetics. Part A
DO  - 10.1002/ajmg.a.70261
UR  - https://doi.org/10.1002/ajmg.a.70261
ER  -

APA

AL, R., GA, A., L, B., N, B., J, C., X, C., Y, C., E, C., S, D., M, F., T, F., D, G., I, G., J, G., KA, K., SB, M., P, M., VK, M., KG, M., SV, M., C, P., L, P., A, R., C, S., K, S., K, S., P, S., T, S., P, T., R, Z., S, Z., & K, I. (2026). Heterozygous Variants in LRP1 Cause a Neurodevelopmental Disorder With Congenital Heart Defects.. American journal of medical genetics. Part A. https://doi.org/10.1002/ajmg.a.70261

Source records

pubmed · retrieved 2026-09-25T15:26:02.019Z
europe-pmc · retrieved 2026-09-25T15:26:02.139Z