reference/29517361

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endingPage	6
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pageRange	334-6
publicationName	The Turkish journal of pediatrics
startingPage	334
bibliographicCitation	Miyamoto T, Yu YS, Sato H, Hayashi H, Sakugawa N, Ishikawa M, Sengoku K. Mutational analysis of the human MBX gene in four Korean families demonstrating microphthalmia with congenital cataract. Turk J Pediatr. 2007 Jul;49(3):334–6. PMID: 17990594.
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date	200707
identifier	https://pubmed.ncbi.nlm.nih.gov/17990594
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/
title	Mutational analysis of the human MBX gene in four Korean families demonstrating microphthalmia with congenital cataract
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Total number of triples: 43.