MMAB, a novel candidate gene to be screened in the molecular diagnosis of Mevalonate Kinase Deficiency
Mevalonate kinase deficiency (MKD) is an autosomal recessive inflammatory disease.
Mutations in MVK gene are associated with MKD with modest genotype–phenotype …
Mutations in MVK gene are associated with MKD with modest genotype–phenotype …
MMAB, a novel candidate gene to be screened in the molecular diagnosis of Mevalonate Kinase Deficiency
M Mezzavilla, RR Moura, F Celsi… - Rheumatology …, 2018 - search.proquest.com
Mevalonate kinase deficiency (MKD) is an autosomal recessive inflammatory disease.
Mutations in MVK gene are associated with MKD with modest genotype–phenotype …
Mutations in MVK gene are associated with MKD with modest genotype–phenotype …
MMAB, a novel candidate gene to be screened in the molecular diagnosis of Mevalonate Kinase Deficiency.
M Mezzavilla, RR Moura, F Celsi… - Rheumatology …, 2017 - europepmc.org
Mevalonate kinase deficiency (MKD) is an autosomal recessive inflammatory disease.
Mutations in MVK gene are associated with MKD with modest genotype-phenotype …
Mutations in MVK gene are associated with MKD with modest genotype-phenotype …
MMAB, a novel candidate gene to be screened in the molecular diagnosis of Mevalonate Kinase Deficiency
M Mezzavilla, RR Moura, F Celsi… - RHEUMATOLOGY …, 2018 - research.unipd.it
Mevalonate kinase deficiency (MKD) is an autosomal recessive inflammatory disease.
Mutations in MVK gene are associated with MKD with modest genotype–phenotype …
Mutations in MVK gene are associated with MKD with modest genotype–phenotype …
MMAB, a novel candidate gene to be screened in the molecular diagnosis of Mevalonate Kinase Deficiency
M Mezzavilla, RR Moura, F Celsi… - Rheumatology …, 2018 - pubmed.ncbi.nlm.nih.gov
Mevalonate kinase deficiency (MKD) is an autosomal recessive inflammatory disease.
Mutations in MVK gene are associated with MKD with modest genotype-phenotype …
Mutations in MVK gene are associated with MKD with modest genotype-phenotype …
MMAB, a novel candidate gene to be screened in the molecular diagnosis of Mevalonate Kinase Deficiency
M Mezzavilla, RR Moura, F CELSI, PM Tricarico… - 2018 - ricerca.unityfvg.it
Mevalonate kinase deficiency (MKD) is an autosomal recessive inflammatory disease.
Mutations in MVK gene are associated with MKD with modest genotype–phenotype …
Mutations in MVK gene are associated with MKD with modest genotype–phenotype …
MMAB, a novel candidate gene to be screened in the molecular diagnosis of Mevalonate Kinase Deficiency
M Mezzavilla, RR Moura, F Celsi, PM Tricarico… - RHEUMATOLOGY …, 2018 - arts.units.it
Mevalonate kinase deficiency (MKD) is an autosomal recessive inflammatory disease.
Mutations in MVK gene are associated with MKD with modest genotype–phenotype …
Mutations in MVK gene are associated with MKD with modest genotype–phenotype …
MMAB, a novel candidate gene to be screened in the molecular diagnosis of Mevalonate Kinase Deficiency.
M Mezzavilla, RR Moura, F Celsi… - Rheumatology …, 2018 - search.ebscohost.com
Mevalonate kinase deficiency (MKD) is an autosomal recessive inflammatory disease.
Mutations in MVK gene are associated with MKD with modest genotype-phenotype …
Mutations in MVK gene are associated with MKD with modest genotype-phenotype …
MMAB, a novel candidate gene to be screened in the molecular diagnosis of Mevalonate Kinase Deficiency
M Mezzavilla, RR Moura, F CELSI, PM Tricarico… - 2018 - ricerca.unityfvg.it
Mevalonate kinase deficiency (MKD) is an autosomal recessive inflammatory disease.
Mutations in MVK gene are associated with MKD with modest genotype–phenotype …
Mutations in MVK gene are associated with MKD with modest genotype–phenotype …