Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals.

Layo-Carris DE, Lubin EE, Sangree AK, Clark KJ, Durham EL, Gonzalez EM, Smith S, Angireddy R, Wang XM, Weiss E, Toutain A, Mendoza-Londono R, Dupuis L, Damseh N, Velasco D, Valenzuela I, Codina-Solà M, Ziats C, Have J, Clarkson K, Steel D, Kurian M, Barwick K, Carrasco D, Dagli AI, Nowaczyk MJM, Hančárová M, Bendová Š, Prchalova D, Sedláček Z, Baxová A, Nowak CB, Douglas J, Chung WK, Longo N, Platzer K, Klöckner C, Averdunk L, Wieczorek D, Krey I, Zweier C, Reis A, Balci T, Simon M, Kroes HY, Wiesener A, Vasileiou G, Marinakis NM, Veltra D, Sofocleous C, Kosma K, Synodinos JT, Voudris KA, Vuillaume ML, Gueguen P, Derive N, Colin E, Battault C, Au B, Delatycki M, Wallis M, Gallacher L, Majdoub F, Smal N, Weckhuysen S, Schoonjans AS, Kooy RF, Meuwissen M, Cocanougher BT, Taylor K, Pizoli CE, McDonald MT, James P, Roeder ER, Littlejohn R, Borja NA, Thorson W, King K, Stoeva R, Suerink M, Nibbeling E, Baskin S, Guyader GLE, Kaplan J, Muss C, Carere DA, Bhoj EJK, Bryant LM

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DOI
10.1038/s41431-024-01659-y
Published
2024 Aug
Container
European journal of human genetics : EJHG
Publisher
Not recorded
Open access
yes

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BibTeX

@article{allodium:10.1038/s41431-024-01659-y,
  title = {Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals.},
  author = {Layo-Carris DE and Lubin EE and Sangree AK and Clark KJ and Durham EL and Gonzalez EM and Smith S and Angireddy R and Wang XM and Weiss E and Toutain A and Mendoza-Londono R and Dupuis L and Damseh N and Velasco D and Valenzuela I and Codina-Solà M and Ziats C and Have J and Clarkson K and Steel D and Kurian M and Barwick K and Carrasco D and Dagli AI and Nowaczyk MJM and Hančárová M and Bendová Š and Prchalova D and Sedláček Z and Baxová A and Nowak CB and Douglas J and Chung WK and Longo N and Platzer K and Klöckner C and Averdunk L and Wieczorek D and Krey I and Zweier C and Reis A and Balci T and Simon M and Kroes HY and Wiesener A and Vasileiou G and Marinakis NM and Veltra D and Sofocleous C and Kosma K and Synodinos JT and Voudris KA and Vuillaume ML and Gueguen P and Derive N and Colin E and Battault C and Au B and Delatycki M and Wallis M and Gallacher L and Majdoub F and Smal N and Weckhuysen S and Schoonjans AS and Kooy RF and Meuwissen M and Cocanougher BT and Taylor K and Pizoli CE and McDonald MT and James P and Roeder ER and Littlejohn R and Borja NA and Thorson W and King K and Stoeva R and Suerink M and Nibbeling E and Baskin S and Guyader GLE and Kaplan J and Muss C and Carere DA and Bhoj EJK and Bryant LM},
  year = {2024},
  journal = {European journal of human genetics : EJHG},
  doi = {10.1038/s41431-024-01659-y},
  url = {https://doi.org/10.1038/s41431-024-01659-y}
}

RIS

TY  - JOUR
TI  - Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals.
AU  - Layo-Carris DE
AU  - Lubin EE
AU  - Sangree AK
AU  - Clark KJ
AU  - Durham EL
AU  - Gonzalez EM
AU  - Smith S
AU  - Angireddy R
AU  - Wang XM
AU  - Weiss E
AU  - Toutain A
AU  - Mendoza-Londono R
AU  - Dupuis L
AU  - Damseh N
AU  - Velasco D
AU  - Valenzuela I
AU  - Codina-Solà M
AU  - Ziats C
AU  - Have J
AU  - Clarkson K
AU  - Steel D
AU  - Kurian M
AU  - Barwick K
AU  - Carrasco D
AU  - Dagli AI
AU  - Nowaczyk MJM
AU  - Hančárová M
AU  - Bendová Š
AU  - Prchalova D
AU  - Sedláček Z
AU  - Baxová A
AU  - Nowak CB
AU  - Douglas J
AU  - Chung WK
AU  - Longo N
AU  - Platzer K
AU  - Klöckner C
AU  - Averdunk L
AU  - Wieczorek D
AU  - Krey I
AU  - Zweier C
AU  - Reis A
AU  - Balci T
AU  - Simon M
AU  - Kroes HY
AU  - Wiesener A
AU  - Vasileiou G
AU  - Marinakis NM
AU  - Veltra D
AU  - Sofocleous C
AU  - Kosma K
AU  - Synodinos JT
AU  - Voudris KA
AU  - Vuillaume ML
AU  - Gueguen P
AU  - Derive N
AU  - Colin E
AU  - Battault C
AU  - Au B
AU  - Delatycki M
AU  - Wallis M
AU  - Gallacher L
AU  - Majdoub F
AU  - Smal N
AU  - Weckhuysen S
AU  - Schoonjans AS
AU  - Kooy RF
AU  - Meuwissen M
AU  - Cocanougher BT
AU  - Taylor K
AU  - Pizoli CE
AU  - McDonald MT
AU  - James P
AU  - Roeder ER
AU  - Littlejohn R
AU  - Borja NA
AU  - Thorson W
AU  - King K
AU  - Stoeva R
AU  - Suerink M
AU  - Nibbeling E
AU  - Baskin S
AU  - Guyader GLE
AU  - Kaplan J
AU  - Muss C
AU  - Carere DA
AU  - Bhoj EJK
AU  - Bryant LM
PY  - 2024
JO  - European journal of human genetics : EJHG
DO  - 10.1038/s41431-024-01659-y
UR  - https://doi.org/10.1038/s41431-024-01659-y
ER  -

APA

DE, L., EE, L., AK, S., KJ, C., EL, D., EM, G., S, S., R, A., XM, W., E, W., A, T., R, M., L, D., N, D., D, V., I, V., M, C., C, Z., J, H., K, C., D, S., M, K., K, B., D, C., AI, D., MJM, N., M, H., Š, B., D, P., Z, S., A, B., CB, N., J, D., WK, C., N, L., K, P., C, K., L, A., D, W., I, K., C, Z., A, R., T, B., M, S., HY, K., A, W., G, V., NM, M., D, V., C, S., K, K., JT, S., KA, V., ML, V., P, G., N, D., E, C., C, B., B, A., M, D., M, W., L, G., F, M., N, S., S, W., AS, S., RF, K., M, M., BT, C., K, T., CE, P., MT, M., P, J., ER, R., R, L., NA, B., W, T., K, K., R, S., M, S., E, N., S, B., GLE, G., J, K., C, M., DA, C., EJK, B., & LM, B. (2024). Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals.. European journal of human genetics : EJHG. https://doi.org/10.1038/s41431-024-01659-y

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