Cite
HARVARD Citation
Watson, C. et al. (2020). Long‐read nanopore sequencing resolves a TMEM231 gene conversion event causing Meckel–Gruber syndrome. Human mutation. 41 (2), pp. 525-531. [Online].
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Watson, C. et al. (2020). Long‐read nanopore sequencing resolves a TMEM231 gene conversion event causing Meckel–Gruber syndrome. Human mutation. 41 (2), pp. 525-531. [Online].