| Predicate |
Object |
| contentType |
Journal Article|Research Support, Non-U.S. Gov't |
| endingPage |
1940 |
| issn |
1552-4833
1552-4825 |
| issueIdentifier |
16 |
| pageRange |
1938-1940 |
| publicationName |
American journal of medical genetics. Part A |
| startingPage |
1938 |
| bibliographicCitation |
Wang H, Nye L, Puffenberger E, Morton H. Phenylalanine hydroxylase deficiency exhibits mutation heterogeneity in two large old order Amish settlements. Am J Med Genet A. 2007 Aug 15;143A(16):1938–40. doi: 10.1002/ajmg.a.31852. PMID: 17630668. |
| creator |
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_157b0f4eea0734a1eca81e2cc05a0888
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_4be320aed0fb81df63d5d2c98076baf2
http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-6388-9148
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_f53cd369396a638b6600c81e391cebfc
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_8289145ac21b38b751a5ad165fb53ba5 |
| date |
2007-07-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| identifier |
https://pubmed.ncbi.nlm.nih.gov/17630668
https://doi.org/10.1002/ajmg.a.31852 |
| isPartOf |
https://portal.issn.org/resource/ISSN/1552-4825
https://portal.issn.org/resource/ISSN/1552-4833
http://rdf.ncbi.nlm.nih.gov/pubchem/journal/32200 |
| language |
English |
| source |
https://www.crossref.org/
https://pubmed.ncbi.nlm.nih.gov/ |
| title |
Phenylalanine hydroxylase deficiency exhibits mutation heterogeneity in two large old order Amish settlements |
| discusses |
http://id.nlm.nih.gov/mesh/M0016546 |
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