DOI: 10.1136/jmg.37.1.50. A connexin 26 mutation causes a syndrome of sensorineural hearing loss and palmoplantar hyperkeratosis (MIM 148350)

A connexin 26 mutation causes a syndrome of sensorineural hearing loss and palmoplantar hyperkeratosis (MIM 148350)

10.1136/jmg.37.1.50

Crossref journal-article

BMJ

Journal of Medical Genetics (239)

Bibliography

Heathcote, K. (2000). A connexin 26 mutation causes a syndrome of sensorineural hearing loss and palmoplantar hyperkeratosis (MIM 148350). Journal of Medical Genetics, 37(1), 50â51.

Authors 1

K. Heathcote (first)

References 0 Referenced 104

None

Dates

Type	When
Created	23 years, 1 month ago (July 27, 2002, 6:37 a.m.)
Deposited	4 years, 11 months ago (Sept. 25, 2020, 11:27 a.m.)
Indexed	4 months, 3 weeks ago (April 6, 2025, 5:42 p.m.)
Issued	25 years, 7 months ago (Jan. 1, 2000)
Published	25 years, 7 months ago (Jan. 1, 2000)
Published Print	25 years, 7 months ago (Jan. 1, 2000)

Funders 0

None

BibTeX

@article{Heathcote_2000, title={A connexin 26 mutation causes a syndrome of sensorineural hearing loss and palmoplantar hyperkeratosis (MIM 148350)}, volume={37}, ISSN={1468-6244}, url={http://dx.doi.org/10.1136/jmg.37.1.50}, DOI={10.1136/jmg.37.1.50}, number={1}, journal={Journal of Medical Genetics}, publisher={BMJ}, author={Heathcote, K.}, year={2000}, month=jan, pages={50–51} }

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