Get the free Mutations in LAMB2 causing a severe form of synaptic congenital ...

Downloaded from http://jmg.bmj.com/ on August 17, 2015, Published by group.bmj.com Mutation report Mutations in LAMB2 causing a severe form of synaptic congenital myasthenia syndrome R A Moselle,1

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What is mutations in lamb2 causing?

Mutations in lamb2 are causing a genetic disorder known as Lamb-Shaffer syndrome.

Who is required to file mutations in lamb2 causing?

Geneticists and researchers studying Lamb-Shaffer syndrome are required to file mutations in lamb2 causing.

How to fill out mutations in lamb2 causing?

To fill out mutations in lamb2 causing, detailed information about the specific mutations identified in the lamb2 gene needs to be documented.

What is the purpose of mutations in lamb2 causing?

The purpose of documenting mutations in lamb2 causing is to advance research on Lamb-Shaffer syndrome and understand its genetic basis.

What information must be reported on mutations in lamb2 causing?

The specific genetic sequence changes identified in the lamb2 gene, along with any associated phenotypic characteristics should be reported on mutations in lamb2 causing.