Functional analysis of PLXNA1 variants in a novel neurodevelopmental syndrome with oculo-cerebral anomalies

EUROPEAN JOURNAL OF HUMAN GENETICS

SPRINGERNATURE

1. NHGRI
2. NHLBI [UM1 HG006542]
3. Herbert-Reeck-foundation
4. [BonnNI:Q-614.2954]
5. [DFG-RE 1723/5-1]
6. [BONFOR:O-120.0001]