A Familial Case of Multicentric Carpotarsal Osteolysis Syndrome and Treatment Outcome

Maria Descartes, et al; Maria Descartes

A Familial Case of Multicentric Carpotarsal Osteolysis Syndrome and Treatment Outcome

Maria Descartes, et al
, Maria Descartes

Research output: Contribution to journal › Article › peer-review

Original language	American English
Journal	Journal of Pediatric Genetics
Volume	7
State	Published - 2018

Disciplines

Medicine and Health Sciences

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@article{9316580300d94933981dd476d6b3cfe1,

title = "A Familial Case of Multicentric Carpotarsal Osteolysis Syndrome and Treatment Outcome",

author = "\{Descartes, et al\}, Maria and Maria Descartes",

note = "Multicentric carpotarsal osteolysis syndrome (MCTO) is a rare skeletal disorder caused by heterozygous mutations in the MAFB gene (v-maf musculoaponeurotic fibrosarcoma oncogene ortholog B). This is an autosomal dominant condition with a high frequency of sporadic cases. MCTO is characterized ...",

year = "2018",

language = "American English",

volume = "7",

journal = "Journal of Pediatric Genetics",

}

TY - JOUR

T1 - A Familial Case of Multicentric Carpotarsal Osteolysis Syndrome and Treatment Outcome

AU - Descartes, et al, Maria

AU - Descartes, Maria

N1 - Multicentric carpotarsal osteolysis syndrome (MCTO) is a rare skeletal disorder caused by heterozygous mutations in the MAFB gene (v-maf musculoaponeurotic fibrosarcoma oncogene ortholog B). This is an autosomal dominant condition with a high frequency of sporadic cases. MCTO is characterized ...

PY - 2018

Y1 - 2018

UR - https://pubmed.ncbi.nlm.nih.gov/30430035/

M3 - Article

VL - 7

JO - Journal of Pediatric Genetics

JF - Journal of Pediatric Genetics

ER -

A Familial Case of Multicentric Carpotarsal Osteolysis Syndrome and Treatment Outcome

Disciplines

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