Gnathodiaphyseal dysplasia presenting as polyostotic fibrous dysplasia

Author:

Vengoechea Jaime1,Carpenter Lori1

Affiliation:

1. Division of Genetics; University of Arkansas for Medical Sciences College of Medicine; Little Rock Arkansas

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference9 articles.

1. Familial cases of new systemic bone disease, hereditary gnatho-diaphyseal sclerosis;Akasaka;Nippon Seikeigeka Gakkai Zasshi,1969

2. Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies;Bolduc;Am J Hum Genet,2010

3. Gnathodiaphyseal dysplasia;Herman;J Perinatol,2014

4. Novel ANO5 homozygous microdeletion causing myalgia and unprovoked rhabdomyolysis in an Arabic man;Lahoria;Muscle Nerve,2014

5. ANO5-muscular dystrophy: clinical, pathological and molecular findings;Liewluck;Eur J Neurol,2013

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