Parmalee et al, 201221
|
Single peak on chromosome 1 at 1q41-42 significant LOD score |
|
Eade et al, 202125
|
Phosphoglycerate dehydrogenase deficiency (PHGDH) on 1p12 locus |
Implicated in glycine and serine metabolism |
Gantner et al, 202126
|
SPTLC1/2 on chromosome 9q22.1-q22.3 |
Associated with hereditary sensory and autonomic neuropathy type 1, may be associated with MacTel |
Bonelli et al, 202127
|
A single nucleotide polymorphism (SNP) at locus 5q14.3 |
Associated with variation in retinal vascular diameter |
Scerri, T. S. et al, 201728
|
CPS 1 on 2q34 locus |
Implicated in glycine and serine metabolism |