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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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G908R NOD2 variant in a family with sarcoidosis

Valérie Besnard1, Alain Calender2, Diane Bouvry3,4

  • 1Université Paris 13, Sorbonne Paris Cité, Laboratoire EA2363 "Hypoxie et Poumon", 74 rue Marcel Cachin, 93017, Bobigny cedex, France. valerie.besnard@univ-paris13.fr.

Respiratory Research
|March 21, 2018
PubMed
Abstract

Keywords:
Familial sarcoidosisGenetic susceptibilityNOD2

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