(Q51161720)

31 March 2018

http://europepmc.org/abstract/MED/24517148

title

A homozygous CaSR mutation causing a FHH phenotype completely masked by vitamin D deficiency presenting as rickets (English)

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31 March 2018

http://europepmc.org/abstract/MED/24517148

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Dorothea Szczawinska

1

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31 March 2018

http://europepmc.org/abstract/MED/24517148

Dirk Schnabel

series ordinal

2

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31 March 2018

http://europepmc.org/abstract/MED/24517148

Saskia Letz

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3

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31 March 2018

http://europepmc.org/abstract/MED/24517148

Christof Schöfl

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4

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31 March 2018

http://europepmc.org/abstract/MED/24517148

language of work or name

English

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publication date

11 February 2014

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31 March 2018

http://europepmc.org/abstract/MED/24517148

published in

The Journal of Clinical Endocrinology and Metabolism

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31 March 2018

http://europepmc.org/abstract/MED/24517148

volume

99

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31 March 2018

http://europepmc.org/abstract/MED/24517148

issue

6

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31 March 2018

http://europepmc.org/abstract/MED/24517148

page(s)

E1146-53

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31 March 2018

http://europepmc.org/abstract/MED/24517148

Identifiers

DOI

10.1210/JC.2013-3593

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31 March 2018

http://europepmc.org/abstract/MED/24517148

1 reference

31 March 2018