Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease.

Teekakirikul P, Zhu W, Gabriel GC, Young CB, Williams K, Martin LJ, Hill JC, Richards T, Billaud M, Phillippi JA, Wang J, Wu Y, Tan T, Devine W, Lin JH, Bais AS, Klonowski J, Moreau de Bellaing A, Saini A, Wang MX, Emerel L, Salamacha N, Wyman SK, Lee C, Sing Li H, Miron A, Zhang J, Xing J, McNamara DM, Fung E, Kirshbom P, Mahle W, Kochilas LK, He Y, Garg V, White P, McBride KL, Benson DW, Gleason TG, Mital S, Lo CW

Open source

DOI
10.1016/j.xhgg.2021.100037
Published
2021 Jul 8
Container
HGG advances
Publisher
Not recorded
Open access
yes

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BibTeX

@article{allodium:10.1016/j.xhgg.2021.100037,
  title = {Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease.},
  author = {Teekakirikul P and Zhu W and Gabriel GC and Young CB and Williams K and Martin LJ and Hill JC and Richards T and Billaud M and Phillippi JA and Wang J and Wu Y and Tan T and Devine W and Lin JH and Bais AS and Klonowski J and Moreau de Bellaing A and Saini A and Wang MX and Emerel L and Salamacha N and Wyman SK and Lee C and Sing Li H and Miron A and Zhang J and Xing J and McNamara DM and Fung E and Kirshbom P and Mahle W and Kochilas LK and He Y and Garg V and White P and McBride KL and Benson DW and Gleason TG and Mital S and Lo CW},
  year = {2021},
  journal = {HGG advances},
  doi = {10.1016/j.xhgg.2021.100037},
  url = {https://doi.org/10.1016/j.xhgg.2021.100037}
}

RIS

TY  - JOUR
TI  - Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease.
AU  - Teekakirikul P
AU  - Zhu W
AU  - Gabriel GC
AU  - Young CB
AU  - Williams K
AU  - Martin LJ
AU  - Hill JC
AU  - Richards T
AU  - Billaud M
AU  - Phillippi JA
AU  - Wang J
AU  - Wu Y
AU  - Tan T
AU  - Devine W
AU  - Lin JH
AU  - Bais AS
AU  - Klonowski J
AU  - Moreau de Bellaing A
AU  - Saini A
AU  - Wang MX
AU  - Emerel L
AU  - Salamacha N
AU  - Wyman SK
AU  - Lee C
AU  - Sing Li H
AU  - Miron A
AU  - Zhang J
AU  - Xing J
AU  - McNamara DM
AU  - Fung E
AU  - Kirshbom P
AU  - Mahle W
AU  - Kochilas LK
AU  - He Y
AU  - Garg V
AU  - White P
AU  - McBride KL
AU  - Benson DW
AU  - Gleason TG
AU  - Mital S
AU  - Lo CW
PY  - 2021
JO  - HGG advances
DO  - 10.1016/j.xhgg.2021.100037
UR  - https://doi.org/10.1016/j.xhgg.2021.100037
ER  -

APA

P, T., W, Z., GC, G., CB, Y., K, W., LJ, M., JC, H., T, R., M, B., JA, P., J, W., Y, W., T, T., W, D., JH, L., AS, B., J, K., A, M. D. B., A, S., MX, W., L, E., N, S., SK, W., C, L., H, S. L., A, M., J, Z., J, X., DM, M., E, F., P, K., W, M., LK, K., Y, H., V, G., P, W., KL, M., DW, B., TG, G., S, M., & CW, L. (2021). Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease.. HGG advances. https://doi.org/10.1016/j.xhgg.2021.100037

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