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 - Springer
Mevalonate kinase deficiency (MKD) is an autosomal recessive inflammatory disease.
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 …

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 …

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 …

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 …

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 …

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 …

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 …

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 …