Blanchard, Stéphane

Defective myosin VIIA gene responsible for Usher syndrome type IB

Well, D., Blanchard, S., Kaplan, J., Guilford, P., Gibson, F., Walsh, J., Mburu, P., Varela, A., Levilliers, J., Weston, M. D., et al. (1995) · Nature

Retinal Development and DisordersGenetic and Kidney Cyst Diseases

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Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome

Hardelin, J.-P., Levilliers, J., Blanchard, S., Carel, J.-C., Leutenegger, M., Pinard-Bertelletto, J.-P., Bouloux, P., & Petit, C. (1993) · Human Molecular Genetics

Hypothalamic control of reproductive hormonesGenetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

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MyRIP, a novel Rab effector, enables myosin VIIa recruitment to retinal melanosomes

El‐Amraoui, A., Schonn, J., Küssel‐Andermann, P., Blanchard, S., Desnos, C., Henry, J., Wolfrum, U., Darchen, F., & Petit, C. (2002) · The EMBO Reports

Cellular transport and secretionRetinal Development and Disorders

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