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Hum Mol Genet
Expanding the phenotype of NUP85 mutations beyond nephrotic syndrome to primary autosomal recessive microcephaly and Seckel syndrome spectrum disorders
- E. Ravindran
- R. Jühlen
- C.H. Vieira-Vieira
- T. Ha
- Y. Salzberg
- B. Fichtman
- L. Luise-Becker
- N. Martins
- S. Picker-Minh
- P. Bessa
- P. Arts
- M.R. Jackson
- A. Taranath
- B. Kamien
- C. Barnett
- N. Li
- V. Tarabykin
- G. Stoltenburg-Didinger
- A. Harel
- M. Selbach
- A. Dickmanns
- B. Fahrenkrog
- H. Hu
- H. Scott
- A.M. Kaindl