Speech and neuromotor retardation, hyperactivity, cranial malformation, seizures

Disease ID:870
Name:Speech and neuromotor retardation, hyperactivity, cranial malformation, seizures
Associated with:1 target

Targets

ADGRL1
References:  1
Mutations:  ADGRL1 is associated with 1 mutation. Click here for details

Ligands

No ligand related data available for Speech and neuromotor retardation, hyperactivity, cranial malformation, seizures

References

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1. Bonaglia MC, Marelli S, Novara F, Commodaro S, Borgatti R, Minardo G, Memo L, Mangold E, Beri S, Zucca C et al.. (2010) Genotype-phenotype relationship in three cases with overlapping 19p13.12 microdeletions. Eur. J. Hum. Genet., 18 (12): 1302-9. [PMID:20648052]