MYD88 L265P mutation contributes to the diagnosis of Bing Neel syndrome.

Poulain, Stéphanie

MYD88 L265P mutation contributes to the diagnosis of Bing Neel syndrome. [electronic resource] - British journal of haematology Nov 2014 - 506-13 p. digital

Publication Type: Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't

1365-2141

10.1111/bjh.13078 doi


Adult
Aged
Bone Marrow--metabolism
Heterozygote
Humans
Male
Middle Aged
Mutation, Missense
Myeloid Differentiation Factor 88--genetics
Neoplasm Proteins--genetics
Nervous System Diseases--cerebrospinal fluid
Prospective Studies
Syndrome
Waldenstrom Macroglobulinemia--cerebrospinal fluid