MG
Michel Guipponi

Publications (2)

X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3
Article scientifique · 2017
Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigree
Article scientifique · 2016

Domaines principaux

Sciences de la vie et biotechnologies2

Statistiques

Consultations4
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