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Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3)

Signal TransductionG Protein-coupled ReceptorGenetic DisorderGeneticsInherited Metabolic DiseaseNovel MutationsMolecular GeneticsDisease Gene IdentificationSystems BiologyMedicineCell SignalingAutosomal Recessive Hypotrichosis