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Article

[OXALATE STONES ARE PREVALENT AMONG DRUZE AND MUSLIM ARABS IN THE GALILEE].

Harefuah - 1 Mar 2017

Kalfon Limor, Weissman Irit, Hershkovits Miriam, Nasser Samra Nadra, Edri Nurit, Khayat Morad, Tanus Mary, Shihab Shihab, Mandel Hanna, Falik-Zaccai Tzipora

Abstract excerpt

INTRODUCTION: Primary Hyperoxaluria type I (PH1) is a rare autosomal recessive disease caused by lack or dysfunction of the liver peroxisomal enzyme alanine: glyoxylate aminotransferase, AGT. AIMS: To conduct clinical and genetic characterization of Druze and Muslim Arab patients with PH1 in Northern Israel. METHODS: In the last 20 years, 36 children and families were diagnosed and treated in the...

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Source

Identifiers

PMID: 28551940

Genes

AGT
AGXT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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