L. Licinio

A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G).

L. Kunkel, M. Schuldiner, M. Zatz, 2014, Human molecular genetics.

Spastic Paraplegia, Optic Atrophy, and Neuropathy: New Observations, Locus Refinement, and Exclusion of Candidate Genes

M. Zatz, A. Pessoa, P. Otto, 2009, Annals of human genetics.

African ancestry protects against Alzheimer's disease-related neuropathology

L. Grinberg, J. Farfel, R. Leite, 2011, Molecular Psychiatry.

Genetic aspects of adolescent idiopathic scoliosis in a family with multiple affected members: a research article

M. Zatz, M. Wajchenberg, D. Martins, 2010, Scoliosis.

Reevaluation of a large family defines a new locus for X-linked recessive pure spastic paraplegia (SPG34) on chromosome Xq25

M. Zatz, F. Kok, S. Santos, 2008, neurogenetics.

Reevaluation of a large family defines a new locus for X-linked recessive pure spastic paraplegia (SPG34) on chromosome Xq25

M. Zatz, F. Kok, R. M. Nascimento, 2008, neurogenetics.

A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G).

L. Kunkel, M. Schuldiner, M. Zatz, 2014, Human molecular genetics.