DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» Hypertryptophanemia
Hypertryptophanemia
Amyloid Like Aggregates Formed by the Self-Assembly of Proline And
Orphanet Report Series Rare Diseases Collection
Omics Knowledgebase for Mammalian Cellular Signaling Pathways
A Defect in Tryptophan Metabolism
The Role of Amino Acids in Neurotransmission and Fluorescent Tools for Their Detection
Geneticists Explore 30-Year Old Medical Case 2 November 2017, by Regina Unger
Whole Exome Sequencing Gene Package Metabolic Disorders, Version 5.1, 31-1-2020
The Use of Gas Chromatography-Mass Spectrometry for the Diagnosis and Study of Metabolic Disorders I
WES Gene Package Metabolic Disorders.Xlsx
ORPHA Number Disease Or Group of Diseases 300305 11P15.4
Formation of Apoptosis‐Inducing Amyloid Fibrils by Tryptophan
Mendeliome Panel Versie V3 (4362 Genen) Centrum Voor Medische Genetica Gent
WES Gene Package Metabolic Disorders.Xlsx
Prevalence and Incidence of Rare Diseases: Bibilographic Data
Metabolite Amyloid-Like Fibrils Interact with Model Membranes
Metabolske Sykdommer V02
Rare Diseases: Unique Assays for Unique Therapies
Source: State: 12.06.2018 ORPHA68367 10507
Top View
Table 3. Disorders in Which Vitamin B6 Preparations
Prevalence and Incidence of Rare Diseases: Bibliographic Data
Prevalence and Incidence of Rare Diseases
List of Rare Diseases and Synonyms
Hormone Profile in Hypersexuality Women
OMIM Mendelian Gene List V2.0
Orphanet Report Series Rare Diseases Collection
WO 2010/144821 Al 16 December 2010 (16.12.2010) PCT