Cite
HARVARD Citation
Fastré, E. et al. (2018). Splice‐site mutations in VEGFC cause loss of function and Nonne‐Milroy‐like primary lymphedema. Clinical genetics. 94 (1), pp. 179-181. [Online].
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Fastré, E. et al. (2018). Splice‐site mutations in VEGFC cause loss of function and Nonne‐Milroy‐like primary lymphedema. Clinical genetics. 94 (1), pp. 179-181. [Online].