A new mutation of ANO6 in two familial cases of Scott syndrome.
Boisseau P, Bene MC, Besnard T, Pachchek S, Giraud M, Talarmain P, Robillard N, Gourlaouen MA, Bezieau S, Fouassier M.
Boisseau P, et al. Among authors: fouassier m.
Br J Haematol. 2018 Mar;180(5):750-752. doi: 10.1111/bjh.14439. Epub 2016 Nov 23.
Br J Haematol. 2018.
PMID: 27879994
Free article.
No abstract available.