Opening book details…
About this Biochemistry, Genetics and Molecular Biology article
Genomic screening in rare disorders: New mutations and phenotypes, highlighting ALG14 as a novel cause of severe intellectual disability by Kvarnung, Malin; Taylan, Fulya; Nilsson, Daniel; Anderlid, Britt-Marie; Malmgren, Helena; Lagerstedt-Robinson, Kristina; Holmberg, Eva; Burstedt, Magnus; Nordenskjöld, Magnus; Nordgren, Ann; Syk Lundberg, Elisabeth is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.
- Author
- Kvarnung, Malin; Taylan, Fulya; Nilsson, Daniel; Anderlid, Britt-Marie; Malmgren, Helena; Lagerstedt-Robinson, Kristina; Holmberg, Eva; Burstedt, Magnus; Nordenskjöld, Magnus; Nordgren, Ann; Syk Lundberg, Elisabeth
- Publisher
- John Wiley and Sons; Wiley (Blackwell Publishing); Blackwell Publishing Inc.; Wiley (ISSN 0009-9163)
- Published
- 2018
- Language
- EN
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)