Erin Loring

Erin Loring

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Erin Loring

Erin Loring

Publications by authors named "Erin Loring"

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Hypokalemia Associated With a Claudin 10 Mutation: A Case Report.

Am J Kidney Dis 2019 Mar 25;73(3):425-428. Epub 2018 Oct 25.

Division of Nephrology, Department of Pediatrics, NYU Langone Health, New York, NY. Electronic address:

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http://dx.doi.org/10.1053/j.ajkd.2018.08.015DOI Listing
March 2019

A novel de novo frameshift mutation in NR0B1 and low prenatal estriol in adrenal hypoplasia congenita.

Ann N Y Acad Sci 2018 12 21;1433(1):7-11. Epub 2018 Aug 21.

Department of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, New York.

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http://dx.doi.org/10.1111/nyas.13962DOI Listing
December 2018

Dominant De Novo Mutations in GJA1 Cause Erythrokeratodermia Variabilis et Progressiva, without Features of Oculodentodigital Dysplasia.

J Invest Dermatol 2015 Jun 14;135(6):1540-1547. Epub 2014 Nov 14.

Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA; Department of Dermatology, Yale University School of Medicine, New Haven, Connecticut, USA; Department of Pathology, Yale University School of Medicine, New Haven, Connecticut, USA. Electronic address:

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http://dx.doi.org/10.1038/jid.2014.485DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4430428PMC
June 2015

Somatic HRAS p.G12S mutation causes woolly hair and epidermal nevi.

J Invest Dermatol 2014 Apr 15;134(4):1149-1152. Epub 2013 Oct 15.

Department of Dermatology, Yale University School of Medicine, New Haven, Connecticut, USA; Department of Pathology, Yale University School of Medicine, New Haven, Connecticut, USA. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S0022202X153672
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http://dx.doi.org/10.1038/jid.2013.430DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3961553PMC
April 2014