The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands

EEA Alders; R Jongbloed; W Deelen; A van den Wijngaard; P Doevendans; Folkert ten Cate; V Regitz-Zagrosek; H-P Vosberg; I van Langen; A Wilde; D Dooijes; M Mannens

doi:10.1016/S0195-668X(03)00466-4

The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands

EEA Alders, R Jongbloed, W Deelen, A van den Wijngaard, P Doevendans, Folkert ten Cate, V Regitz-Zagrosek, H-P Vosberg, I van Langen, A Wilde, D Dooijes, M Mannens

Research output: Contribution to journal › Article › Academic › peer-review

123 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	1848-1853
Number of pages	6
Journal	European Heart Journal
Volume	24
DOIs	https://doi.org/10.1016/S0195-668X(03)00466-4
Publication status	Published - 2003

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10.1016/S0195-668X(03)00466-4

http://hdl.handle.net/1765/68056

Cite this

Alders, EEA., Jongbloed, R., Deelen, W., van den Wijngaard, A., Doevendans, P., ten Cate, F., Regitz-Zagrosek, V., Vosberg, H-P., van Langen, I., Wilde, A., Dooijes, D., & Mannens, M. (2003). The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands. European Heart Journal, 24, 1848-1853. https://doi.org/10.1016/S0195-668X(03)00466-4

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title = "The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands",

author = "EEA Alders and R Jongbloed and W Deelen and {van den Wijngaard}, A and P Doevendans and {ten Cate}, Folkert and V Regitz-Zagrosek and H-P Vosberg and {van Langen}, I and A Wilde and D Dooijes and M Mannens",

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doi = "10.1016/S0195-668X(03)00466-4",

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Alders, EEA, Jongbloed, R, Deelen, W, van den Wijngaard, A, Doevendans, P, ten Cate, F, Regitz-Zagrosek, V, Vosberg, H-P, van Langen, I, Wilde, A, Dooijes, D & Mannens, M 2003, 'The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands', European Heart Journal, vol. 24, pp. 1848-1853. https://doi.org/10.1016/S0195-668X(03)00466-4

TY - JOUR

T1 - The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands

AU - Alders, EEA

AU - Jongbloed, R

AU - Deelen, W

AU - van den Wijngaard, A

AU - Doevendans, P

AU - ten Cate, Folkert

AU - Regitz-Zagrosek, V

AU - Vosberg, H-P

AU - van Langen, I

AU - Wilde, A

AU - Dooijes, D

AU - Mannens, M

PY - 2003

Y1 - 2003

U2 - 10.1016/S0195-668X(03)00466-4

DO - 10.1016/S0195-668X(03)00466-4

M3 - Article

VL - 24

SP - 1848

EP - 1853

JO - European Heart Journal

JF - European Heart Journal

SN - 0195-668X

ER -