Justine Rousselot

Publication Activity (10 Years)

Years Active: 2024-2024
Publications (10 Years): 6

Top Topics

Iron Deficiency

Intellectual Disability

Genome Wide Identification

Top Venues

This page only lists publications with an associated author ORCID identifier.

Publications

Yoann Vial, Jeannette Nardelli, Adeline A Bonnard, Justine Rousselot, Michèle Souyri, Pierre Gressens, Hélène Cave, Séverine Drunat
Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis. EMBO reports 25 (5) (2024)
Yoann Vial, Jeannette Nardelli, Adeline A Bonnard, Justine Rousselot, Michèle Souyri, Pierre Gressens, Hélène Cave, Séverine Drunat
Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis. EMBO reports 25 (5) (2024)
Yoann Vial, Jeannette Nardelli, Adeline A Bonnard, Justine Rousselot, Michèle Souyri, Pierre Gressens, Hélène Cave, Séverine Drunat
Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis. EMBO reports 25 (5) (2024)
Yoann Vial, Jeannette Nardelli, Adeline A Bonnard, Justine Rousselot, Michèle Souyri, Pierre Gressens, Hélène Cave, Séverine Drunat
Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis. EMBO reports 25 (5) (2024)
Yoann Vial, Jeannette Nardelli, Adeline A Bonnard, Justine Rousselot, Michèle Souyri, Pierre Gressens, Hélène Cave, Séverine Drunat
Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis. EMBO reports (2024)
Yoann Vial, Jeannette Nardelli, Adeline A Bonnard, Justine Rousselot, Michèle Souyri, Pierre Gressens, Hélène Cave, Séverine Drunat
Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis. EMBO reports 25 (5) (2024)