Congenital factor XIII deficiency in Switzerland: From the worldwide first case in 1960 to its molecular characterisation in 2005

V Schroeder; E Meili; G Schubiger

doi:10.4414/smw.2007.11756

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Vol. 137 No. 1920 (2007)

Congenital factor XIII deficiency in Switzerland: From the worldwide first case in 1960 to its molecular characterisation in 2005

V Schroeder
E Meili
G Schubiger

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DOI: https://doi.org/10.4414/smw.2007.11756
Cite this as:: Swiss Med Wkly. 2007;137:272-278
Published: 19.05.2007

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1.

Schroeder V, Meili E, Schubiger G. Congenital factor XIII deficiency in Switzerland: From the worldwide first case in 1960 to its molecular characterisation in 2005. Swiss Med Wkly [Internet]. 2007 May 19 [cited 2024 Nov. 19];137(1920):272-8. Available from: https://smw.ch/index.php/smw/article/view/733

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