No. of disease causing mutations: 1
| Identifier | Nucleotide change | Mutation | Amino acid change/
Predicted consequence |
Location | Restriction site change | Reference |
|---|---|---|---|---|---|---|
| mcln6.001 | c.307insC | 1-bp insertion | Frameshift after P102 | exon 4 | Wheeler et al. 2002 Am J Hum Genet 70: 537-542 Gao et al. 2002. Am J Hum Genet 70: 324-335 |