Skip to main content
Fig. 3 | BMC Neurology

Fig. 3

From: A novel RAB39B mutation and concurrent de novo NF1 mutation in a boy with neurofibromatosis type 1, intellectual disability, and autism: a case report

Fig. 3

3D homology modeling. The 3D homology model (RefSeq: NP_741995.1; residues 1–213) was generated based on the available Rab-8A model (RCS-PDB: 5SZI; residues 1–209) for wild-type and mutant form. a Deleted residues (GMKY) are highlighted in magenta, and flanking residues (Y145; I150) in yellow. b The GTP/Mg2+ binding site is highlighted in red

Back to article page

BMC Neurology

ISSN: 1471-2377

Contact us