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| 1 |
Phenylketonuria: Current Treatments and Future Developments
Lee, Jeongho;
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The Korea Society of Inherited Metabolic Disease
, v.20, no.2, pp.37-43,
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| 2 |
Hypocalcemic Tetany in a 10-year Old Boy: A Case of Pseudohypoparathyroidism Type 1b due to Paternal Uniparental Disomy
Yoo, Byung Min;Kim, Mijin;Ko, Jung Min;Kang, Min Jae;
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The Korea Society of Inherited Metabolic Disease
, v.20, no.2, pp.44-49,
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| 3 |
Vici Syndrome with Novel Compound Heterozygous Mutations in EPG5
Shin, Jehee;Lee, Hyunjoo;Lee, Young-Mock;
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The Korea Society of Inherited Metabolic Disease
, v.20, no.2, pp.50-54,
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| 4 |
Chronic Hereditary Tyrosinemia Type I with Novel Mutation in FAH Gene
Yang, Sungmin;Choi, Hyo Won;Kang, Yun Koo;Lee, Jin-Sung;Namgoong, Mee Kyung;
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The Korea Society of Inherited Metabolic Disease
, v.20, no.2, pp.55-62,
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