DOI:
10.1055/s-00000077
Seminars in Thrombosis and Hemostasis
LinksClose Window
References
Ksantini M, Lafont E, Bocquet B, Meunier I, Hamel CP.
Homozygous mutation in MERTK causes severe autosomal recessive retinitis pigmentosa.
Eur J Ophthalmol 2012;
22 (04) 647-653
We do not assume any responsibility for the contents of the web pages of other providers.