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Cell Press, American Journal of Human Genetics, 3(96), p. 412-424, 2015

DOI: 10.1016/j.ajhg.2015.01.013

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Mutations in the NHEJ component XRCC4 cause primordial dwarfism

Journal article published in 2015 by Jennie E. Murray, Mirjam van der Burg, Hanna IJspeert, Paula Carroll, Qian Wu, Takashi Ochi, Andrea Leitch, Edward S. Miller, Boris Kysela, Alireza Jawad, Armand Bottani, Francesco Brancati, Marco Cappa, Valerie Cormier-Daire ORCID, Charu Deshpande and other authors.
This paper is available in a repository.
This paper is available in a repository.

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