Publications (10) Publications in which a researcher has participated

filter_list Genetics

2014

  1. Mutations in EMP2 cause childhood-onset Nephrotic syndrome

    American Journal of Human Genetics, Vol. 94, Núm. 6, pp. 884-890

2013

  1. ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6

    American Journal of Human Genetics, Vol. 93, Núm. 2, pp. 336-345