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
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]