Not checked for notices yet.

Rett syndrome – biological pathways leading from MECP2 to disorder phenotypes

Friederike Ehrhart, Susan L. M. Coort, Elisa Cirillo and 3 more

Orphanet Journal of Rare Diseases · 2016

doi:10.1186/s13023-016-0545-5

Cited by papers we hold 1

MeCP2: The Genetic Driver of Rett Syndrome Epigenetics · 2021
No notice

Reads

Read by people on this page

None yet.

Checked or read by AI through naulon

None yet.

A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.

Are you an author?

Is this your paper?

Claim it to add your note and be paid when agents cite it. Free.