NARA Discovery
Article Details
← Back to Search Results
Journal Article

De novo variants in GREB1L are associated with non-syndromic inner ear malformations and deafness

Isabelle Schrauwen; Elina Kari; Jacob Mattox; Lorida Llaci; Joanna Smeeton; Marcus Naymik; David W. Raible; James A. Knowles; J. Gage Crump; Matthew J. Huentelman; Rick A. Friedman
Human Genetics · Vol. 137, Issue 6-7 · pp. 459-470 · 2018

Abstract

Abstract is unavailable.

Bibliographic Information

JournalHuman Genetics
PublisherSpringer
Publication Date2018-07-01
Publication Year2018
Volume137
Issue6-7
Pages459-470
Document TypeJournal Article
Print ISSN0340-6717
eISSN1432-1203
DOI10.1007/s00439-018-1898-8

Access Information

NARA Access Coverage1964-01-01~Current
Journal Homepagehttps://www.springer.com/journal/439
Publisher PageOpen Publisher Page
Full-text access depends on NARA's subscribed coverage and institutional access.