B. HAERTER Et Al. , "Early Clinical Diagnosis of PC1/3 Deficiency in a Patient With a Novel Homozygous PCSK1 Splice-Site Mutation," JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION , vol.62, no.4, pp.577-580, 2016
HAERTER, B. Et Al. 2016. Early Clinical Diagnosis of PC1/3 Deficiency in a Patient With a Novel Homozygous PCSK1 Splice-Site Mutation. JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION , vol.62, no.4 , 577-580.
HAERTER, B., FUCHS, I., MUELLER, T., Akbulut, U. E., ÇAKIR, M., & JANECKE, A. R., (2016). Early Clinical Diagnosis of PC1/3 Deficiency in a Patient With a Novel Homozygous PCSK1 Splice-Site Mutation. JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION , vol.62, no.4, 577-580.
HAERTER, Bettina Et Al. "Early Clinical Diagnosis of PC1/3 Deficiency in a Patient With a Novel Homozygous PCSK1 Splice-Site Mutation," JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION , vol.62, no.4, 577-580, 2016
HAERTER, Bettina Et Al. "Early Clinical Diagnosis of PC1/3 Deficiency in a Patient With a Novel Homozygous PCSK1 Splice-Site Mutation." JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION , vol.62, no.4, pp.577-580, 2016
HAERTER, B. Et Al. (2016) . "Early Clinical Diagnosis of PC1/3 Deficiency in a Patient With a Novel Homozygous PCSK1 Splice-Site Mutation." JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION , vol.62, no.4, pp.577-580.
@article{article, author={Bettina HAERTER Et Al. }, title={Early Clinical Diagnosis of PC1/3 Deficiency in a Patient With a Novel Homozygous PCSK1 Splice-Site Mutation}, journal={JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION}, year=2016, pages={577-580} }