RPLP0 and Charcot-Marie-Tooth disease axonal type 2L: The morphants of the rplp0 gene, whose human ortholog is included in the candidate chromosomal region of Charcot-Marie-Tooth disease type 2L (CMT2L, a type of neuropathy; OMIM 608673), showed hypoplasia of the rhombencephalon that is strongly correlated with motor functioning (see the database: http://zebrafish.med.miyazaki-u.ac.jp).