Genetic Polymorphisms in the ESR1 and VDR Genes Do Not Correlate With Osteoporosis in Patients With Familial Dysautonomia-Reference-Cited by-同舟云学术

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Genetic Polymorphisms in the ESR1 and VDR Genes Do Not Correlate With Osteoporosis in Patients With Familial Dysautonomia

Published:2018-04 Issue:2 Volume:21 Page:205-212
ISSN:1094-6950
Container-title:Journal of Clinical Densitometry
language:en
Short-container-title:Journal of Clinical Densitometry

Author:

Cheishvili David,Maayan Channa,Sapozhnikov Daniel M.,Lax Elad,Dresner-Pollak Rivka

Publisher

Elsevier BV

Subject

Radiology, Nuclear Medicine and imaging,Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Reference32 articles.

1. Incidence of familial dysautonomia in Israel 1977–1981;Maayan;Clin Genet,1987

2. Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia;Slaugenhaupt;Am J Hum Genet,2001

3. Familial dysautonomia is caused by mutations of the IKAP gene;Anderson;Am J Hum Genet,2001

4. IKAP/hELP1 deficiency in the cerebrum of familial dysautonomia patients results in down regulation of genes involved in oligodendrocyte differentiation and in myelination;Cheishvili;Hum Mol Genet,2007

5. Familial dysautonomia;Axelrod,2000

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