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A Novel Homozygous Missense Mutation in SLURP1 Causing Mal de Meleda With an Atypical Phenotype

Gruber, R., Hennies, Hans C., Romani, N. and Schmuth, M. (2011) A Novel Homozygous Missense Mutation in SLURP1 Causing Mal de Meleda With an Atypical Phenotype. Archives of Dermatology, 147 (6). pp. 748-750. ISSN 0003-987X
Information
URI:
https://eprints.hud.ac.uk/id/eprint/28777
Title:
A Novel Homozygous Missense Mutation in SLURP1 Causing Mal de Meleda With an Atypical Phenotype
Creators:
Gruber, R., Hennies, Hans C., Romani, N. and Schmuth, M.
Identification Number:
https://doi.org/10.1001/archdermatol.2011.138
Official URL:
http://dx.doi.org/10.1001/archdermatol.2011.138
Date:
20 June 2011
Subjects:
Q Science > QH Natural history > QH301 Biology
Q Science > QH Natural history > QH426 Genetics
Schools:
School of Applied Sciences
Additional Information:
Unmapped bibliographic data: ST - A Novel Homozygous Missense Mutation in SLURP1 Causing Mal de Meleda With an Atypical Phenotype [Field not mapped to EPrints] LB - 84 [Field not mapped to EPrints] RP - Not in File [Field not mapped to EPrints]
Uncontrolled Keywords:
Missense
Library
Item Type:
Article
Depositing User:
Hans Hennies
Date Deposited:
11 Jul 2016 15:04
Revision:
10
Last Modified:
28 Aug 2021 12:05
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