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Functional characterization of the human myosin-7a motor domain

Functional characterization of the human myosin-7a motor domain

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3249170

Functional characterization of the human myosin-7a motor domain

About this item

Full title

Functional characterization of the human myosin-7a motor domain

Publisher

Basel: SP Birkhäuser Verlag Basel

Journal title

Cellular and molecular life sciences : CMLS, 2012-01, Vol.69 (2), p.299-311

Language

English

Formats

Publication information

Publisher

Basel: SP Birkhäuser Verlag Basel

More information

Scope and Contents

Contents

Myosin-7a participates in auditory and visual processes. Defects in
MYO7A
, the gene encoding the myosin-7a heavy chain, are causative for Usher syndrome 1B, the most frequent cause of deaf-blindness in humans. In the present study, we performed a detailed kinetic and functional characterization of the isolated human myosin-7a motor domain to...

Alternative Titles

Full title

Functional characterization of the human myosin-7a motor domain

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3249170

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3249170

Other Identifiers

ISSN

1420-682X

E-ISSN

1420-9071

DOI

10.1007/s00018-011-0749-8

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