Bi-allelic loss-of-function variants in LTBP1cause autosomal recessive cutis laxa syndrome
(2022)
EUROPEAN JOURNAL OF HUMAN GENETICS.
In European Journal of Human Genetics
30(supplement 1).
p.40-41
- Author
- Lore Pottie (UGent) , Christin S. Adamo, Aude Beyens (UGent) , Steffen Luetke, Piyanoot Tapaneeyaphan (UGent) , Adelbert De Clercq (UGent) , Phil Salmon, Riet De Rycke (UGent) , Alper Gezdirici, Elif Yilmaz Gulec, Naz Khan, Jill E. Urquhart, William G. Newman, Kay Metcalfe, Stephanie Efthymiou, Reza Maroofian, Najwa Anwar, Shazia Maqbool, Fatima Rahman, Ikhlass Altweijri, Monerah Alsaleh, Sawsan Mohamed Abdullah, Mohammad Al-Owain, Mais Hashem, Henry Houlden, Fowzan S. Alkuraya, Patrick Sips (UGent) , Gerhard Sengle and Bert Callewaert (UGent)
- Organization
Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-8761611
- MLA
- Pottie, Lore, et al. “Bi-Allelic Loss-of-Function Variants in LTBP1cause Autosomal Recessive Cutis Laxa Syndrome.” EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 30, no. supplement 1, 2022, pp. 40–41.
- APA
- Pottie, L., Adamo, C. S., Beyens, A., Luetke, S., Tapaneeyaphan, P., De Clercq, A., … Callewaert, B. (2022). Bi-allelic loss-of-function variants in LTBP1cause autosomal recessive cutis laxa syndrome. EUROPEAN JOURNAL OF HUMAN GENETICS, 30(supplement 1), 40–41.
- Chicago author-date
- Pottie, Lore, Christin S. Adamo, Aude Beyens, Steffen Luetke, Piyanoot Tapaneeyaphan, Adelbert De Clercq, Phil Salmon, et al. 2022. “Bi-Allelic Loss-of-Function Variants in LTBP1cause Autosomal Recessive Cutis Laxa Syndrome.” In EUROPEAN JOURNAL OF HUMAN GENETICS, 30:40–41.
- Chicago author-date (all authors)
- Pottie, Lore, Christin S. Adamo, Aude Beyens, Steffen Luetke, Piyanoot Tapaneeyaphan, Adelbert De Clercq, Phil Salmon, Riet De Rycke, Alper Gezdirici, Elif Yilmaz Gulec, Naz Khan, Jill E. Urquhart, William G. Newman, Kay Metcalfe, Stephanie Efthymiou, Reza Maroofian, Najwa Anwar, Shazia Maqbool, Fatima Rahman, Ikhlass Altweijri, Monerah Alsaleh, Sawsan Mohamed Abdullah, Mohammad Al-Owain, Mais Hashem, Henry Houlden, Fowzan S. Alkuraya, Patrick Sips, Gerhard Sengle, and Bert Callewaert. 2022. “Bi-Allelic Loss-of-Function Variants in LTBP1cause Autosomal Recessive Cutis Laxa Syndrome.” In EUROPEAN JOURNAL OF HUMAN GENETICS, 30:40–41.
- Vancouver
- 1.Pottie L, Adamo CS, Beyens A, Luetke S, Tapaneeyaphan P, De Clercq A, et al. Bi-allelic loss-of-function variants in LTBP1cause autosomal recessive cutis laxa syndrome. In: EUROPEAN JOURNAL OF HUMAN GENETICS. 2022. p. 40–1.
- IEEE
- [1]L. Pottie et al., “Bi-allelic loss-of-function variants in LTBP1cause autosomal recessive cutis laxa syndrome,” in EUROPEAN JOURNAL OF HUMAN GENETICS, Online, 2022, vol. 30, no. supplement 1, pp. 40–41.
@inproceedings{8761611,
articleno = {{C08.2}},
author = {{Pottie, Lore and Adamo, Christin S. and Beyens, Aude and Luetke, Steffen and Tapaneeyaphan, Piyanoot and De Clercq, Adelbert and Salmon, Phil and De Rycke, Riet and Gezdirici, Alper and Gulec, Elif Yilmaz and Khan, Naz and Urquhart, Jill E. and Newman, William G. and Metcalfe, Kay and Efthymiou, Stephanie and Maroofian, Reza and Anwar, Najwa and Maqbool, Shazia and Rahman, Fatima and Altweijri, Ikhlass and Alsaleh, Monerah and Abdullah, Sawsan Mohamed and Al-Owain, Mohammad and Hashem, Mais and Houlden, Henry and Alkuraya, Fowzan S. and Sips, Patrick and Sengle, Gerhard and Callewaert, Bert}},
booktitle = {{EUROPEAN JOURNAL OF HUMAN GENETICS}},
issn = {{1018-4813}},
language = {{eng}},
location = {{Online}},
number = {{supplement 1}},
pages = {{C08.2:40--C08.2:41}},
title = {{Bi-allelic loss-of-function variants in LTBP1cause autosomal recessive cutis laxa syndrome}},
volume = {{30}},
year = {{2022}},
}