Cite
HARVARD Citation
Flusser, H. et al. (2018). Novel SBF1 splice‐site null mutation broadens the clinical spectrum of Charcot‐Marie‐Tooth type 4B3 disease. Clinical genetics. 94 (5), pp. 473-479. [Online].
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Flusser, H. et al. (2018). Novel SBF1 splice‐site null mutation broadens the clinical spectrum of Charcot‐Marie‐Tooth type 4B3 disease. Clinical genetics. 94 (5), pp. 473-479. [Online].