LONP1 Variants Are Associated With Clinically Diverse Phenotypes.

Young RE, Qiao L, Hernan R, Sweetser DA, Waxler JL, Scott DA, Scott TM, Lalani SR, Azamian MS, Rosenfeld JA, Bostwick B, Burrage LC, Undiagnosed Diseases Network, Rodan LH, Russell BE, Dutra-Clarke M, Kruer M, Bakhtiarim S, Darvish H, Amor DJ, Rahman S, Stals K, Bradley L, Byrne S, Tolusso LK, Wong B, Benedict L, Wallis K, Micke K, Colson C, Smol T, Southwick SV, Miller KA, Kush ML, Chorin O, Rothschild A, Wang W, Shen Y, Chung WK

Open source

DOI: 10.1111/cge.70057
Published: 2026 Mar
Container: Clinical genetics
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1111/cge.70057,
  title = {LONP1 Variants Are Associated With Clinically Diverse Phenotypes.},
  author = {Young RE and Qiao L and Hernan R and Sweetser DA and Waxler JL and Scott DA and Scott TM and Lalani SR and Azamian MS and Rosenfeld JA and Bostwick B and Burrage LC and Undiagnosed Diseases Network and Rodan LH and Russell BE and Dutra-Clarke M and Kruer M and Bakhtiarim S and Darvish H and Amor DJ and Rahman S and Stals K and Bradley L and Byrne S and Tolusso LK and Wong B and Benedict L and Wallis K and Micke K and Colson C and Smol T and Southwick SV and Miller KA and Kush ML and Chorin O and Rothschild A and Wang W and Shen Y and Chung WK},
  year = {2026},
  journal = {Clinical genetics},
  doi = {10.1111/cge.70057},
  url = {https://doi.org/10.1111/cge.70057}
}

RIS

TY  - JOUR
TI  - LONP1 Variants Are Associated With Clinically Diverse Phenotypes.
AU  - Young RE
AU  - Qiao L
AU  - Hernan R
AU  - Sweetser DA
AU  - Waxler JL
AU  - Scott DA
AU  - Scott TM
AU  - Lalani SR
AU  - Azamian MS
AU  - Rosenfeld JA
AU  - Bostwick B
AU  - Burrage LC
AU  - Undiagnosed Diseases Network
AU  - Rodan LH
AU  - Russell BE
AU  - Dutra-Clarke M
AU  - Kruer M
AU  - Bakhtiarim S
AU  - Darvish H
AU  - Amor DJ
AU  - Rahman S
AU  - Stals K
AU  - Bradley L
AU  - Byrne S
AU  - Tolusso LK
AU  - Wong B
AU  - Benedict L
AU  - Wallis K
AU  - Micke K
AU  - Colson C
AU  - Smol T
AU  - Southwick SV
AU  - Miller KA
AU  - Kush ML
AU  - Chorin O
AU  - Rothschild A
AU  - Wang W
AU  - Shen Y
AU  - Chung WK
PY  - 2026
JO  - Clinical genetics
DO  - 10.1111/cge.70057
UR  - https://doi.org/10.1111/cge.70057
ER  -

APA

RE, Y., L, Q., R, H., DA, S., JL, W., DA, S., TM, S., SR, L., MS, A., JA, R., B, B., LC, B., Network, U. D., LH, R., BE, R., M, D., M, K., S, B., H, D., DJ, A., S, R., K, S., L, B., S, B., LK, T., B, W., L, B., K, W., K, M., C, C., T, S., SV, S., KA, M., ML, K., O, C., A, R., W, W., Y, S., & WK, C. (2026). LONP1 Variants Are Associated With Clinically Diverse Phenotypes.. Clinical genetics. https://doi.org/10.1111/cge.70057

Source records

pubmed · retrieved 2026-09-27T12:15:54.062Z