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

por Aswath, Nalini, Swamikannu, Bhuminathan, Ramakrishnan, Sankar Narayanan, Shanmugam, Rajendran, Thomas, Jayakar, Ramanathan, Arvind
Publicado 2014