z-logo
Premium
Novel mutation of the TINF2 gene resulting in severe phenotypic Revesz syndrome
Author(s) -
Sakwit Anusak,
Rojanaporn Duangnate,
Mekjaruskul Pimsiri,
Suriyajakryuththana Wiboon,
Sasanakul Werasak,
Sirachainan gnuch
Publication year - 2019
Publication title -
pediatric blood and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.116
H-Index - 105
eISSN - 1545-5017
pISSN - 1545-5009
DOI - 10.1002/pbc.27557
Subject(s) - medicine , phenotype , genetics , mutation , gene , biology

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom