Cite
HARVARD Citation
Chartier, S. et al. (2018). A neuropathological study of novel RTTN gene mutations causing a familial microcephaly with simplified gyral pattern. Birth defects research. 110 (7), pp. 598-602. [Online].
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Chartier, S. et al. (2018). A neuropathological study of novel RTTN gene mutations causing a familial microcephaly with simplified gyral pattern. Birth defects research. 110 (7), pp. 598-602. [Online].