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Clinical characteristics and phenotype-genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations

✍ Scribed by Demirbilek, H.; Arya, V. B.; Ozbek, M. N.; Akinci, A.; Dogan, M.; Demirel, F.; Houghton, J.; Kaba, S.; Guzel, F.; Baran, R. T.; Unal, S.; Tekkes, S.; Flanagan, S. E.; Ellard, S.; Hussain, K.

Book ID: 121861153
Publisher: Bioscientifica
Year: 2014
Tongue: English
Weight: 136 KB
Volume: 170
Category: Article
ISSN: 0804-4643
DOI: 10.1530/EJE-14-0045

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