Cutis laxa and excessive bone growth due to de novo mutations in PTDSS1. (2018)
Attributed to:
Investigating phosphatidylserine metabolism in Lenz-Majewski syndrome
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1002/ajmg.a.38604
PubMed Identifier: 29341480
Publication URI: http://europepmc.org/abstract/MED/29341480
Type: Journal Article/Review
Volume: 176
Parent Publication: American journal of medical genetics. Part A
Issue: 3
ISSN: 1552-4825