Identification of a novel mutation confirms the implication of IFT172 (BBS20) in Bardet–Biedl syndrome - Concepedia

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Identification of a novel mutation confirms the implication of IFT172 (BBS20) in Bardet–Biedl syndrome

70

Citations

14

References

2016

Year

Élise Schaefer, Corinne Stoetzel, Sophie Scheidecker, Véronique Geoffroy, Megana Prasad, Claire Redin, Isabelle Missotte, Didier Lacombe, Jean‐Louis Mandel, Jean Muller,

Journal of Human Genetics

Novel MutationMendelian DisorderAutoimmune DiseaseGenetic DisorderGeneticsInherited Metabolic DiseasePathologyBardet–biedl SyndromeMolecular GeneticsDisease Gene IdentificationMedicine

References

	Year	Citations

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