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Hannah M Mitchison — latest news, discussion & facts — IJR
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Hannah M Mitchison
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researcher
Hannah M Mitchison
British cell biologist
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About Hannah M Mitchison
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researcher
Website
http://iris.ucl.ac.uk/iris/browse/profile?upi=HMMIT79
Family
Avrion Mitchison
father
Lorna Margaret Martin
mother
Related
Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities
known for
Primary ciliary dyskinesia: current state of the art.
known for
Diagnosis and management of primary ciliary dyskinesia
known for
Mutations in ZMYND10, a gene essential for proper axonemal assembly of inner and outer dynein arms in humans and flies, cause primary ciliary dyskinesia
known for
Splice-site mutations in the axonemal outer dynein arm docking complex gene CCDC114 cause primary ciliary dyskinesia
known for
Mutations in CCDC39 and CCDC40 are the major cause of primary ciliary dyskinesia with axonemal disorganization and absent inner dynein arms
known for
Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement
known for
X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3.
known for
University College London
employer
Related journals
Family
Avrion Mitchison
Lorna Margaret Martin
Connected
Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities
Primary ciliary dyskinesia: current state of the art.
Diagnosis and management of primary ciliary dyskinesia
Mutations in ZMYND10, a gene essential for proper axonemal assembly of inner and outer dynein arms in humans and flies, cause primary ciliary dyskinesia
Splice-site mutations in the axonemal outer dynein arm docking complex gene CCDC114 cause primary ciliary dyskinesia
Mutations in CCDC39 and CCDC40 are the major cause of primary ciliary dyskinesia with axonemal disorganization and absent inner dynein arms
Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement
X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3.
University College London
