Premium
Clinical insights and molecular study of three foetuses with DYNC2H1 gene mutation causing short rib thoracic dystrophy
Author(s) -
Thakur Seema,
Gupta Rachna,
Bansal Deepak,
Singh Chanchal,
Agarwal Divya,
Saxena Kamal Kant
Publication year - 2021
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/cge.13953
Subject(s) - mutation , genetics , gene , muscular dystrophy , biology , dystrophy , medicine , bioinformatics
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom