Publications by authors named "L Garbes"

Claim this Profile
A
Autosomal-Recessive Mutations in MESD Cause Osteogenesis Imperfecta.
Shahida Moosa, Guilherme L Yamamoto, Lutz Garbes, Katharina Keupp, Ana Beleza-Meireles

Am J Hum Genet· October 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Neurocalcin Delta Suppression Protects against Spinal Muscular Atrophy in Humans and across Species by Restoring Impaired Endocytosis.
Markus Riessland, Anna Kaczmarek, Svenja Schneider, Kathryn J Swoboda, Heiko Löhr, Lutz Garbes

Am J Hum Genet· February 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations in SEC24D, encoding a component of the COPII machinery, cause a syndromic form of osteogenesis imperfecta.
Lutz Garbes, Kyungho Kim, Angelika Rieß, Heike Hoyer-Kuhn, Filippo Beleggia

Am J Hum Genet· March 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A paucisymptomatic neuromuscular disease mimicking type III 5q-SMA with complex rearrangements in the SMN gene.
Laura Nanna Lohkamp, Katja von Au, Hans-Hilmar Goebel, Wolfram Kress, Ulrike Grieben, Lutz Garbes

J Child Neurol· February 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
RAD51C deletion screening identifies a recurrent gross deletion in breast cancer and ovarian cancer families.
Gioia Schnurbein, Jan Hauke, Barbara Wappenschmidt, Nana Weber-Lassalle, Stefanie Engert, Lutz Garbes

Breast Cancer Res· December 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis