Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Abigail Loh
Recurrent De Novo Mutations Affecting Residue Arg138 of Pyrroline-5-Carboxylate Synthase Cause a Progeroid Form of Autosomal-Dominant Cutis Laxa
American Journal of Human Genetics
Genetics
Related publications
Autosomal Dominant Cutis Laxa
Mutation in Pyrroline-5-Carboxylate Reductase 1 Gene in Families With Cutis Laxa Type 2
American Journal of Human Genetics
Genetics
Autosomal Recessive Cutis Laxa Type 2B
Congenital Cutis Laxa With a Dominant Inheritance and Early Onset Emphysema.
Thorax
Pulmonary
Respiratory Medicine
Mutations in SEC63 Cause Autosomal Dominant Polycystic Liver Disease
Nature Genetics
Genetics
Mutations in KCNJ13 Cause Autosomal-Dominant Snowflake Vitreoretinal Degeneration
American Journal of Human Genetics
Genetics
Pyrroline-5-Carboxylate Reductase in Human Erythrocytes.
Journal of Clinical Investigation
Medicine
Pyrroline-5-Carboxylate Reductase 1 (PYCR1)
Science-Business eXchange
Cutis Laxa: A Feature of Costello Syndrome.
Journal of Medical Genetics
Genetics