Aswath, N., Swamikannu, B., Ramakrishnan, S. N., Shanmugam, R., Thomas, J., & Ramanathan, A. (2014). Heterozygous Ile453Val codon mutation in exon 7, homozygous single nucleotide polymorphisms in intron 2 and 5 of cathepsin C are associated with Haim-Munk syndrome. Medknow Publications & Media Pvt Ltd.

Aswath, Nalini, Bhuminathan Swamikannu, Sankar Narayanan Ramakrishnan, Rajendran Shanmugam, Jayakar Thomas, and Arvind Ramanathan. Heterozygous Ile453Val Codon Mutation in Exon 7, Homozygous Single Nucleotide Polymorphisms in Intron 2 and 5 of Cathepsin C Are Associated With Haim-Munk Syndrome. Medknow Publications & Media Pvt Ltd, 2014.

Aswath, Nalini, et al. Heterozygous Ile453Val Codon Mutation in Exon 7, Homozygous Single Nucleotide Polymorphisms in Intron 2 and 5 of Cathepsin C Are Associated With Haim-Munk Syndrome. Medknow Publications & Media Pvt Ltd, 2014.