Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation - Concepedia

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Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation

DOI Full Paper Access

32

Citations

27

References

2008

Year

Lynn Petukhova, Edilson C. Sousa, Amalia Martı́nez-Mir, Anna Vitebsky, Lina Gomes dos Santos, Lawrence Shapiro, Chad Haynes, Derek Gordon, Yutaka Shimomura, Angela M. Christiano

Genome-wide Linkage AnalysisMendelian DisorderGenetic DisorderGeneticsMolecular GeneticsDisease Gene IdentificationNovel P2ry5 MutationGenomicsSystems BiologyMedicineAutosomal Recessive Hypotrichosis

References

	Year	Citations

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