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
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