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A Missense Mutation of C1659 in the Fibroblast Growth Factor Receptor 3 Gene in Russian Patients with Hypochondroplasia
by
FOFANOVA, OLGA V.
,
TAKAMURA, NOBORU
,
KINOSHITA, EI-ICHI
,
MEERSON, ELENA M.
,
ILJINA, VALENTINA K.
,
NECHVOLODOVA, OLGA L.
,
EVGRAFOV, OLEG V.
,
PETERKOVA, VALENTINA A.
,
YAMASHITA, SHUNICHI
Published in
Endocrine Journal
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A Missense Mutation of C1659 in the Fibroblast Growth Factor Receptor 3 Gene in Russian Patients with Hypochondroplasia
by
OLGA V. FOFANOVA
,
NOBORU TAKAMURA
,
EI-ICHI KINOSHITA
,
ELENA M. MEERSON
,
VALENTINA K. ILJINA
,
OLGA L. NECHVOLODOVA
,
OLEG V. EVGRAFOV
,
VALENTINA A. PETERKOVA
,
SHUNICHI YAMASHITA
,
#
Published in
ENDOCRINE JOURNAL
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Endocrine Journal
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Subjects
Fgfr3 Gene
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Fibroblast Growth Factor Receptor 3
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Hypochondroplasia
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Adolescent
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Adult
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Child, Preschool
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Endocrinology & Metabolism
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Female
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Humans
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Life Sciences & Biomedicine
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Middle Aged
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Mutation, Missense
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Osteochondrodysplasias - Genetics
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Phenotype
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Protein-Tyrosine Kinases - Chemistry
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Receptor, Fibroblast Growth Factor, Type 3
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Receptors, Fibroblast Growth Factor - Chemistry
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Receptors, Fibroblast Growth Factor - Genetics
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